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Items: 1 to 20 of 291

1.

rs1489190887 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    9:110941721 (GRCh38)
    9:113704001 (GRCh37)
    Canonical SPDI:
    NC_000009.12:110941720:C:G
    Gene:
    LPAR1 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    G=0.000007/1 (GnomAD)
    G=0.000019/5 (TOPMED)
    HGVS:
    NC_000009.12:g.110941721C>G, NC_000009.11:g.113704001C>G, NM_001401.5:c.493G>C, NM_001401.4:c.493G>C, NM_001401.3:c.493G>C, NM_057159.4:c.493G>C, NM_057159.3:c.493G>C, NM_057159.2:c.493G>C, NM_001351410.2:c.493G>C, NM_001351410.1:c.493G>C, NM_001351409.2:c.493G>C, NM_001351409.1:c.493G>C, NM_001351407.2:c.493G>C, NM_001351407.1:c.493G>C, NM_001351413.2:c.493G>C, NM_001351413.1:c.493G>C, NM_001351412.2:c.493G>C, NM_001351412.1:c.493G>C, NM_001351408.2:c.493G>C, NM_001351408.1:c.493G>C, NM_001351415.2:c.493G>C, NM_001351415.1:c.493G>C, NM_001351418.2:c.493G>C, NM_001351418.1:c.493G>C, NM_001351414.2:c.493G>C, NM_001351414.1:c.493G>C, NM_001351416.2:c.493G>C, NM_001351416.1:c.493G>C, NM_001351411.2:c.493G>C, NM_001351411.1:c.493G>C, NM_001351417.2:c.493G>C, NM_001351417.1:c.493G>C, NM_001351398.2:c.493G>C, NM_001351398.1:c.493G>C, NM_001351401.2:c.493G>C, NM_001351401.1:c.493G>C, NM_001351406.2:c.493G>C, NM_001351406.1:c.493G>C, NM_001351400.2:c.493G>C, NM_001351400.1:c.493G>C, NM_001351420.2:c.493G>C, NM_001351420.1:c.493G>C, NM_001351399.2:c.493G>C, NM_001351399.1:c.493G>C, NM_001351402.2:c.493G>C, NM_001351402.1:c.493G>C, NM_001351419.2:c.493G>C, NM_001351419.1:c.493G>C, NM_001351405.2:c.493G>C, NM_001351405.1:c.493G>C, NM_001351404.2:c.493G>C, NM_001351404.1:c.493G>C, NM_001351397.2:c.493G>C, NM_001351397.1:c.493G>C, NM_001351403.2:c.493G>C, NM_001351403.1:c.493G>C, NM_001387494.1:c.493G>C, NM_001387490.1:c.493G>C, NM_001387492.1:c.493G>C, NM_001387501.1:c.493G>C, NM_001387498.1:c.493G>C, NM_001387512.1:c.493G>C, NM_001387513.1:c.493G>C, NM_001387505.1:c.493G>C, NM_001387489.1:c.493G>C, NM_001387508.1:c.493G>C, NM_001387495.1:c.493G>C, NM_001387509.1:c.493G>C, NM_001387517.1:c.439G>C, NM_001387496.1:c.493G>C, NM_001387484.1:c.493G>C, NM_001387491.1:c.493G>C, NM_001387507.1:c.493G>C, NM_001387506.1:c.493G>C, NM_001387473.1:c.493G>C, XM_047422903.1:c.493G>C, NM_001387511.1:c.493G>C, NM_001387487.1:c.493G>C, NM_001387479.1:c.493G>C, NM_001387483.1:c.493G>C, NM_001387474.1:c.493G>C, NM_001387502.1:c.493G>C, NM_001387510.1:c.493G>C, NM_001387504.1:c.493G>C, NM_001387478.1:c.493G>C, NM_001387488.1:c.493G>C, NM_001387493.1:c.493G>C, NM_001387476.1:c.493G>C, NM_001387477.1:c.493G>C, NM_001387503.1:c.493G>C, NM_001387497.1:c.493G>C, NM_001387516.1:c.439G>C, NM_001387480.1:c.493G>C, NM_001387470.1:c.493G>C, NM_001387472.1:c.493G>C, NM_001387475.1:c.493G>C, NM_001387486.1:c.493G>C, NM_001387482.1:c.493G>C, NM_001387481.1:c.493G>C, NM_001387515.1:c.493G>C, NM_001387518.1:c.439G>C, NM_001387471.1:c.493G>C, NM_001387485.1:c.493G>C, NM_001387514.1:c.493G>C, NM_001387521.1:c.493G>C, NM_001387520.1:c.493G>C, NM_001387519.1:c.493G>C, NP_001392.2:p.Val165Leu, NP_476500.1:p.Val165Leu, NP_001338339.1:p.Val165Leu, NP_001338338.1:p.Val165Leu, NP_001338336.1:p.Val165Leu, NP_001338342.1:p.Val165Leu, NP_001338341.1:p.Val165Leu, NP_001338337.1:p.Val165Leu, NP_001338344.1:p.Val165Leu, NP_001338347.1:p.Val165Leu, NP_001338343.1:p.Val165Leu, NP_001338345.1:p.Val165Leu, NP_001338340.1:p.Val165Leu, NP_001338346.1:p.Val165Leu, NP_001338327.1:p.Val165Leu, NP_001338330.1:p.Val165Leu, NP_001338335.1:p.Val165Leu, NP_001338329.1:p.Val165Leu, NP_001338349.1:p.Val165Leu, NP_001338328.1:p.Val165Leu, NP_001338331.1:p.Val165Leu, NP_001338348.1:p.Val165Leu, NP_001338334.1:p.Val165Leu, NP_001338333.1:p.Val165Leu, NP_001338326.1:p.Val165Leu, NP_001338332.1:p.Val165Leu, NP_001374423.1:p.Val165Leu, NP_001374419.1:p.Val165Leu, NP_001374421.1:p.Val165Leu, NP_001374430.1:p.Val165Leu, NP_001374427.1:p.Val165Leu, NP_001374441.1:p.Val165Leu, NP_001374442.1:p.Val165Leu, NP_001374434.1:p.Val165Leu, NP_001374418.1:p.Val165Leu, NP_001374437.1:p.Val165Leu, NP_001374424.1:p.Val165Leu, NP_001374438.1:p.Val165Leu, NP_001374446.1:p.Val147Leu, NP_001374425.1:p.Val165Leu, NP_001374413.1:p.Val165Leu, NP_001374420.1:p.Val165Leu, NP_001374436.1:p.Val165Leu, NP_001374435.1:p.Val165Leu, NP_001374402.1:p.Val165Leu, XP_047278859.1:p.Val165Leu, NP_001374440.1:p.Val165Leu, NP_001374416.1:p.Val165Leu, NP_001374408.1:p.Val165Leu, NP_001374412.1:p.Val165Leu, NP_001374403.1:p.Val165Leu, NP_001374431.1:p.Val165Leu, NP_001374439.1:p.Val165Leu, NP_001374433.1:p.Val165Leu, NP_001374407.1:p.Val165Leu, NP_001374417.1:p.Val165Leu, NP_001374422.1:p.Val165Leu, NP_001374405.1:p.Val165Leu, NP_001374406.1:p.Val165Leu, NP_001374432.1:p.Val165Leu, NP_001374426.1:p.Val165Leu, NP_001374445.1:p.Val147Leu, NP_001374409.1:p.Val165Leu, NP_001374399.1:p.Val165Leu, NP_001374401.1:p.Val165Leu, NP_001374404.1:p.Val165Leu, NP_001374415.1:p.Val165Leu, NP_001374411.1:p.Val165Leu, NP_001374410.1:p.Val165Leu, NP_001374444.1:p.Val165Leu, NP_001374447.1:p.Val147Leu, NP_001374400.1:p.Val165Leu, NP_001374414.1:p.Val165Leu, NP_001374443.1:p.Val165Leu, NP_001374450.1:p.Val165Leu, NP_001374449.1:p.Val165Leu, NP_001374448.1:p.Val165Leu

    2.

    rs1486201037 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>A [Show Flanks]
      Chromosome:
      9:110941774 (GRCh38)
      9:113704054 (GRCh37)
      Canonical SPDI:
      NC_000009.12:110941773:T:A
      Gene:
      LPAR1 (Varview)
      Functional Consequence:
      coding_sequence_variant,missense_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0./0 (ALFA)
      A=0.000004/1 (TOPMED)
      HGVS:
      NC_000009.12:g.110941774T>A, NC_000009.11:g.113704054T>A, NM_001401.5:c.440A>T, NM_001401.4:c.440A>T, NM_001401.3:c.440A>T, NM_057159.4:c.440A>T, NM_057159.3:c.440A>T, NM_057159.2:c.440A>T, NM_001351410.2:c.440A>T, NM_001351410.1:c.440A>T, NM_001351409.2:c.440A>T, NM_001351409.1:c.440A>T, NM_001351407.2:c.440A>T, NM_001351407.1:c.440A>T, NM_001351413.2:c.440A>T, NM_001351413.1:c.440A>T, NM_001351412.2:c.440A>T, NM_001351412.1:c.440A>T, NM_001351408.2:c.440A>T, NM_001351408.1:c.440A>T, NM_001351415.2:c.440A>T, NM_001351415.1:c.440A>T, NM_001351418.2:c.440A>T, NM_001351418.1:c.440A>T, NM_001351414.2:c.440A>T, NM_001351414.1:c.440A>T, NM_001351416.2:c.440A>T, NM_001351416.1:c.440A>T, NM_001351411.2:c.440A>T, NM_001351411.1:c.440A>T, NM_001351417.2:c.440A>T, NM_001351417.1:c.440A>T, NM_001351398.2:c.440A>T, NM_001351398.1:c.440A>T, NM_001351401.2:c.440A>T, NM_001351401.1:c.440A>T, NM_001351406.2:c.440A>T, NM_001351406.1:c.440A>T, NM_001351400.2:c.440A>T, NM_001351400.1:c.440A>T, NM_001351420.2:c.440A>T, NM_001351420.1:c.440A>T, NM_001351399.2:c.440A>T, NM_001351399.1:c.440A>T, NM_001351402.2:c.440A>T, NM_001351402.1:c.440A>T, NM_001351419.2:c.440A>T, NM_001351419.1:c.440A>T, NM_001351405.2:c.440A>T, NM_001351405.1:c.440A>T, NM_001351404.2:c.440A>T, NM_001351404.1:c.440A>T, NM_001351397.2:c.440A>T, NM_001351397.1:c.440A>T, NM_001351403.2:c.440A>T, NM_001351403.1:c.440A>T, NM_001387494.1:c.440A>T, NM_001387490.1:c.440A>T, NM_001387492.1:c.440A>T, NM_001387501.1:c.440A>T, NM_001387498.1:c.440A>T, NM_001387512.1:c.440A>T, NM_001387513.1:c.440A>T, NM_001387505.1:c.440A>T, NM_001387489.1:c.440A>T, NM_001387508.1:c.440A>T, NM_001387495.1:c.440A>T, NM_001387509.1:c.440A>T, NM_001387517.1:c.386A>T, NM_001387496.1:c.440A>T, NM_001387484.1:c.440A>T, NM_001387491.1:c.440A>T, NM_001387507.1:c.440A>T, NM_001387506.1:c.440A>T, NM_001387473.1:c.440A>T, XM_047422903.1:c.440A>T, NM_001387511.1:c.440A>T, NM_001387487.1:c.440A>T, NM_001387479.1:c.440A>T, NM_001387483.1:c.440A>T, NM_001387474.1:c.440A>T, NM_001387502.1:c.440A>T, NM_001387510.1:c.440A>T, NM_001387504.1:c.440A>T, NM_001387478.1:c.440A>T, NM_001387488.1:c.440A>T, NM_001387493.1:c.440A>T, NM_001387476.1:c.440A>T, NM_001387477.1:c.440A>T, NM_001387503.1:c.440A>T, NM_001387497.1:c.440A>T, NM_001387516.1:c.386A>T, NM_001387480.1:c.440A>T, NM_001387470.1:c.440A>T, NM_001387472.1:c.440A>T, NM_001387475.1:c.440A>T, NM_001387486.1:c.440A>T, NM_001387482.1:c.440A>T, NM_001387481.1:c.440A>T, NM_001387515.1:c.440A>T, NM_001387518.1:c.386A>T, NM_001387471.1:c.440A>T, NM_001387485.1:c.440A>T, NM_001387514.1:c.440A>T, NM_001387521.1:c.440A>T, NM_001387520.1:c.440A>T, NM_001387519.1:c.440A>T, NP_001392.2:p.His147Leu, NP_476500.1:p.His147Leu, NP_001338339.1:p.His147Leu, NP_001338338.1:p.His147Leu, NP_001338336.1:p.His147Leu, NP_001338342.1:p.His147Leu, NP_001338341.1:p.His147Leu, NP_001338337.1:p.His147Leu, NP_001338344.1:p.His147Leu, NP_001338347.1:p.His147Leu, NP_001338343.1:p.His147Leu, NP_001338345.1:p.His147Leu, NP_001338340.1:p.His147Leu, NP_001338346.1:p.His147Leu, NP_001338327.1:p.His147Leu, NP_001338330.1:p.His147Leu, NP_001338335.1:p.His147Leu, NP_001338329.1:p.His147Leu, NP_001338349.1:p.His147Leu, NP_001338328.1:p.His147Leu, NP_001338331.1:p.His147Leu, NP_001338348.1:p.His147Leu, NP_001338334.1:p.His147Leu, NP_001338333.1:p.His147Leu, NP_001338326.1:p.His147Leu, NP_001338332.1:p.His147Leu, NP_001374423.1:p.His147Leu, NP_001374419.1:p.His147Leu, NP_001374421.1:p.His147Leu, NP_001374430.1:p.His147Leu, NP_001374427.1:p.His147Leu, NP_001374441.1:p.His147Leu, NP_001374442.1:p.His147Leu, NP_001374434.1:p.His147Leu, NP_001374418.1:p.His147Leu, NP_001374437.1:p.His147Leu, NP_001374424.1:p.His147Leu, NP_001374438.1:p.His147Leu, NP_001374446.1:p.His129Leu, NP_001374425.1:p.His147Leu, NP_001374413.1:p.His147Leu, NP_001374420.1:p.His147Leu, NP_001374436.1:p.His147Leu, NP_001374435.1:p.His147Leu, NP_001374402.1:p.His147Leu, XP_047278859.1:p.His147Leu, NP_001374440.1:p.His147Leu, NP_001374416.1:p.His147Leu, NP_001374408.1:p.His147Leu, NP_001374412.1:p.His147Leu, NP_001374403.1:p.His147Leu, NP_001374431.1:p.His147Leu, NP_001374439.1:p.His147Leu, NP_001374433.1:p.His147Leu, NP_001374407.1:p.His147Leu, NP_001374417.1:p.His147Leu, NP_001374422.1:p.His147Leu, NP_001374405.1:p.His147Leu, NP_001374406.1:p.His147Leu, NP_001374432.1:p.His147Leu, NP_001374426.1:p.His147Leu, NP_001374445.1:p.His129Leu, NP_001374409.1:p.His147Leu, NP_001374399.1:p.His147Leu, NP_001374401.1:p.His147Leu, NP_001374404.1:p.His147Leu, NP_001374415.1:p.His147Leu, NP_001374411.1:p.His147Leu, NP_001374410.1:p.His147Leu, NP_001374444.1:p.His147Leu, NP_001374447.1:p.His129Leu, NP_001374400.1:p.His147Leu, NP_001374414.1:p.His147Leu, NP_001374443.1:p.His147Leu, NP_001374450.1:p.His147Leu, NP_001374449.1:p.His147Leu, NP_001374448.1:p.His147Leu

      3.

      rs1480207610 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C,G [Show Flanks]
        Chromosome:
        9:110941879 (GRCh38)
        9:113704159 (GRCh37)
        Canonical SPDI:
        NC_000009.12:110941878:T:C,NC_000009.12:110941878:T:G
        Gene:
        LPAR1 (Varview)
        Functional Consequence:
        coding_sequence_variant,missense_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        G=0.000004/1 (GnomAD_exomes)
        G=0.000014/2 (GnomAD)
        C=0.000035/1 (TOMMO)
        HGVS:
        NC_000009.12:g.110941879T>C, NC_000009.12:g.110941879T>G, NC_000009.11:g.113704159T>C, NC_000009.11:g.113704159T>G, NM_001401.5:c.335A>G, NM_001401.5:c.335A>C, NM_001401.4:c.335A>G, NM_001401.4:c.335A>C, NM_001401.3:c.335A>G, NM_001401.3:c.335A>C, NM_057159.4:c.335A>G, NM_057159.4:c.335A>C, NM_057159.3:c.335A>G, NM_057159.3:c.335A>C, NM_057159.2:c.335A>G, NM_057159.2:c.335A>C, NM_001351410.2:c.335A>G, NM_001351410.2:c.335A>C, NM_001351410.1:c.335A>G, NM_001351410.1:c.335A>C, NM_001351409.2:c.335A>G, NM_001351409.2:c.335A>C, NM_001351409.1:c.335A>G, NM_001351409.1:c.335A>C, NM_001351407.2:c.335A>G, NM_001351407.2:c.335A>C, NM_001351407.1:c.335A>G, NM_001351407.1:c.335A>C, NM_001351413.2:c.335A>G, NM_001351413.2:c.335A>C, NM_001351413.1:c.335A>G, NM_001351413.1:c.335A>C, NM_001351412.2:c.335A>G, NM_001351412.2:c.335A>C, NM_001351412.1:c.335A>G, NM_001351412.1:c.335A>C, NM_001351408.2:c.335A>G, NM_001351408.2:c.335A>C, NM_001351408.1:c.335A>G, NM_001351408.1:c.335A>C, NM_001351415.2:c.335A>G, NM_001351415.2:c.335A>C, NM_001351415.1:c.335A>G, NM_001351415.1:c.335A>C, NM_001351418.2:c.335A>G, NM_001351418.2:c.335A>C, NM_001351418.1:c.335A>G, NM_001351418.1:c.335A>C, NM_001351414.2:c.335A>G, NM_001351414.2:c.335A>C, NM_001351414.1:c.335A>G, NM_001351414.1:c.335A>C, NM_001351416.2:c.335A>G, NM_001351416.2:c.335A>C, NM_001351416.1:c.335A>G, NM_001351416.1:c.335A>C, NM_001351411.2:c.335A>G, NM_001351411.2:c.335A>C, NM_001351411.1:c.335A>G, NM_001351411.1:c.335A>C, NM_001351417.2:c.335A>G, NM_001351417.2:c.335A>C, NM_001351417.1:c.335A>G, NM_001351417.1:c.335A>C, NM_001351398.2:c.335A>G, NM_001351398.2:c.335A>C, NM_001351398.1:c.335A>G, NM_001351398.1:c.335A>C, NM_001351401.2:c.335A>G, NM_001351401.2:c.335A>C, NM_001351401.1:c.335A>G, NM_001351401.1:c.335A>C, NM_001351406.2:c.335A>G, NM_001351406.2:c.335A>C, NM_001351406.1:c.335A>G, NM_001351406.1:c.335A>C, NM_001351400.2:c.335A>G, NM_001351400.2:c.335A>C, NM_001351400.1:c.335A>G, NM_001351400.1:c.335A>C, NM_001351420.2:c.335A>G, NM_001351420.2:c.335A>C, NM_001351420.1:c.335A>G, NM_001351420.1:c.335A>C, NM_001351399.2:c.335A>G, NM_001351399.2:c.335A>C, NM_001351399.1:c.335A>G, NM_001351399.1:c.335A>C, NM_001351402.2:c.335A>G, NM_001351402.2:c.335A>C, NM_001351402.1:c.335A>G, NM_001351402.1:c.335A>C, NM_001351419.2:c.335A>G, NM_001351419.2:c.335A>C, NM_001351419.1:c.335A>G, NM_001351419.1:c.335A>C, NM_001351405.2:c.335A>G, NM_001351405.2:c.335A>C, NM_001351405.1:c.335A>G, NM_001351405.1:c.335A>C, NM_001351404.2:c.335A>G, NM_001351404.2:c.335A>C, NM_001351404.1:c.335A>G, NM_001351404.1:c.335A>C, NM_001351397.2:c.335A>G, NM_001351397.2:c.335A>C, NM_001351397.1:c.335A>G, NM_001351397.1:c.335A>C, NM_001351403.2:c.335A>G, NM_001351403.2:c.335A>C, NM_001351403.1:c.335A>G, NM_001351403.1:c.335A>C, NM_001387494.1:c.335A>G, NM_001387494.1:c.335A>C, NM_001387490.1:c.335A>G, NM_001387490.1:c.335A>C, NM_001387492.1:c.335A>G, NM_001387492.1:c.335A>C, NM_001387501.1:c.335A>G, NM_001387501.1:c.335A>C, NM_001387498.1:c.335A>G, NM_001387498.1:c.335A>C, NM_001387512.1:c.335A>G, NM_001387512.1:c.335A>C, NM_001387513.1:c.335A>G, NM_001387513.1:c.335A>C, NM_001387505.1:c.335A>G, NM_001387505.1:c.335A>C, NM_001387489.1:c.335A>G, NM_001387489.1:c.335A>C, NM_001387508.1:c.335A>G, NM_001387508.1:c.335A>C, NM_001387495.1:c.335A>G, NM_001387495.1:c.335A>C, NM_001387509.1:c.335A>G, NM_001387509.1:c.335A>C, NM_001387517.1:c.281A>G, NM_001387517.1:c.281A>C, NM_001387496.1:c.335A>G, NM_001387496.1:c.335A>C, NM_001387484.1:c.335A>G, NM_001387484.1:c.335A>C, NM_001387491.1:c.335A>G, NM_001387491.1:c.335A>C, NM_001387507.1:c.335A>G, NM_001387507.1:c.335A>C, NM_001387506.1:c.335A>G, NM_001387506.1:c.335A>C, NM_001387473.1:c.335A>G, NM_001387473.1:c.335A>C, XM_047422903.1:c.335A>G, XM_047422903.1:c.335A>C, NM_001387511.1:c.335A>G, NM_001387511.1:c.335A>C, NM_001387487.1:c.335A>G, NM_001387487.1:c.335A>C, NM_001387479.1:c.335A>G, NM_001387479.1:c.335A>C, NM_001387483.1:c.335A>G, NM_001387483.1:c.335A>C, NM_001387474.1:c.335A>G, NM_001387474.1:c.335A>C, NM_001387502.1:c.335A>G, NM_001387502.1:c.335A>C, NM_001387510.1:c.335A>G, NM_001387510.1:c.335A>C, NM_001387504.1:c.335A>G, NM_001387504.1:c.335A>C, NM_001387478.1:c.335A>G, NM_001387478.1:c.335A>C, NM_001387488.1:c.335A>G, NM_001387488.1:c.335A>C, NM_001387493.1:c.335A>G, NM_001387493.1:c.335A>C, NM_001387476.1:c.335A>G, NM_001387476.1:c.335A>C, NM_001387477.1:c.335A>G, NM_001387477.1:c.335A>C, NM_001387503.1:c.335A>G, NM_001387503.1:c.335A>C, NM_001387497.1:c.335A>G, NM_001387497.1:c.335A>C, NM_001387516.1:c.281A>G, NM_001387516.1:c.281A>C, NM_001387480.1:c.335A>G, NM_001387480.1:c.335A>C, NM_001387470.1:c.335A>G, NM_001387470.1:c.335A>C, NM_001387472.1:c.335A>G, NM_001387472.1:c.335A>C, NM_001387475.1:c.335A>G, NM_001387475.1:c.335A>C, NM_001387486.1:c.335A>G, NM_001387486.1:c.335A>C, NM_001387482.1:c.335A>G, NM_001387482.1:c.335A>C, NM_001387481.1:c.335A>G, NM_001387481.1:c.335A>C, NM_001387515.1:c.335A>G, NM_001387515.1:c.335A>C, NM_001387518.1:c.281A>G, NM_001387518.1:c.281A>C, NM_001387471.1:c.335A>G, NM_001387471.1:c.335A>C, NM_001387485.1:c.335A>G, NM_001387485.1:c.335A>C, NM_001387514.1:c.335A>G, NM_001387514.1:c.335A>C, NM_001387521.1:c.335A>G, NM_001387521.1:c.335A>C, NM_001387520.1:c.335A>G, NM_001387520.1:c.335A>C, NM_001387519.1:c.335A>G, NM_001387519.1:c.335A>C, NP_001392.2:p.Asn112Ser, NP_001392.2:p.Asn112Thr, NP_476500.1:p.Asn112Ser, NP_476500.1:p.Asn112Thr, NP_001338339.1:p.Asn112Ser, NP_001338339.1:p.Asn112Thr, NP_001338338.1:p.Asn112Ser, NP_001338338.1:p.Asn112Thr, NP_001338336.1:p.Asn112Ser, NP_001338336.1:p.Asn112Thr, NP_001338342.1:p.Asn112Ser, NP_001338342.1:p.Asn112Thr, NP_001338341.1:p.Asn112Ser, NP_001338341.1:p.Asn112Thr, NP_001338337.1:p.Asn112Ser, NP_001338337.1:p.Asn112Thr, NP_001338344.1:p.Asn112Ser, NP_001338344.1:p.Asn112Thr, NP_001338347.1:p.Asn112Ser, NP_001338347.1:p.Asn112Thr, NP_001338343.1:p.Asn112Ser, NP_001338343.1:p.Asn112Thr, NP_001338345.1:p.Asn112Ser, NP_001338345.1:p.Asn112Thr, NP_001338340.1:p.Asn112Ser, NP_001338340.1:p.Asn112Thr, NP_001338346.1:p.Asn112Ser, NP_001338346.1:p.Asn112Thr, NP_001338327.1:p.Asn112Ser, NP_001338327.1:p.Asn112Thr, NP_001338330.1:p.Asn112Ser, NP_001338330.1:p.Asn112Thr, NP_001338335.1:p.Asn112Ser, NP_001338335.1:p.Asn112Thr, NP_001338329.1:p.Asn112Ser, NP_001338329.1:p.Asn112Thr, NP_001338349.1:p.Asn112Ser, NP_001338349.1:p.Asn112Thr, NP_001338328.1:p.Asn112Ser, NP_001338328.1:p.Asn112Thr, NP_001338331.1:p.Asn112Ser, NP_001338331.1:p.Asn112Thr, NP_001338348.1:p.Asn112Ser, NP_001338348.1:p.Asn112Thr, NP_001338334.1:p.Asn112Ser, NP_001338334.1:p.Asn112Thr, NP_001338333.1:p.Asn112Ser, NP_001338333.1:p.Asn112Thr, NP_001338326.1:p.Asn112Ser, NP_001338326.1:p.Asn112Thr, NP_001338332.1:p.Asn112Ser, NP_001338332.1:p.Asn112Thr, NP_001374423.1:p.Asn112Ser, NP_001374423.1:p.Asn112Thr, NP_001374419.1:p.Asn112Ser, NP_001374419.1:p.Asn112Thr, NP_001374421.1:p.Asn112Ser, NP_001374421.1:p.Asn112Thr, NP_001374430.1:p.Asn112Ser, NP_001374430.1:p.Asn112Thr, NP_001374427.1:p.Asn112Ser, NP_001374427.1:p.Asn112Thr, NP_001374441.1:p.Asn112Ser, NP_001374441.1:p.Asn112Thr, NP_001374442.1:p.Asn112Ser, NP_001374442.1:p.Asn112Thr, NP_001374434.1:p.Asn112Ser, NP_001374434.1:p.Asn112Thr, NP_001374418.1:p.Asn112Ser, NP_001374418.1:p.Asn112Thr, NP_001374437.1:p.Asn112Ser, NP_001374437.1:p.Asn112Thr, NP_001374424.1:p.Asn112Ser, NP_001374424.1:p.Asn112Thr, NP_001374438.1:p.Asn112Ser, NP_001374438.1:p.Asn112Thr, NP_001374446.1:p.Asn94Ser, NP_001374446.1:p.Asn94Thr, NP_001374425.1:p.Asn112Ser, NP_001374425.1:p.Asn112Thr, NP_001374413.1:p.Asn112Ser, NP_001374413.1:p.Asn112Thr, NP_001374420.1:p.Asn112Ser, NP_001374420.1:p.Asn112Thr, NP_001374436.1:p.Asn112Ser, NP_001374436.1:p.Asn112Thr, NP_001374435.1:p.Asn112Ser, NP_001374435.1:p.Asn112Thr, NP_001374402.1:p.Asn112Ser, NP_001374402.1:p.Asn112Thr, XP_047278859.1:p.Asn112Ser, XP_047278859.1:p.Asn112Thr, NP_001374440.1:p.Asn112Ser, NP_001374440.1:p.Asn112Thr, NP_001374416.1:p.Asn112Ser, NP_001374416.1:p.Asn112Thr, NP_001374408.1:p.Asn112Ser, NP_001374408.1:p.Asn112Thr, NP_001374412.1:p.Asn112Ser, NP_001374412.1:p.Asn112Thr, NP_001374403.1:p.Asn112Ser, NP_001374403.1:p.Asn112Thr, NP_001374431.1:p.Asn112Ser, NP_001374431.1:p.Asn112Thr, NP_001374439.1:p.Asn112Ser, NP_001374439.1:p.Asn112Thr, NP_001374433.1:p.Asn112Ser, NP_001374433.1:p.Asn112Thr, NP_001374407.1:p.Asn112Ser, NP_001374407.1:p.Asn112Thr, NP_001374417.1:p.Asn112Ser, NP_001374417.1:p.Asn112Thr, NP_001374422.1:p.Asn112Ser, NP_001374422.1:p.Asn112Thr, NP_001374405.1:p.Asn112Ser, NP_001374405.1:p.Asn112Thr, NP_001374406.1:p.Asn112Ser, NP_001374406.1:p.Asn112Thr, NP_001374432.1:p.Asn112Ser, NP_001374432.1:p.Asn112Thr, NP_001374426.1:p.Asn112Ser, NP_001374426.1:p.Asn112Thr, NP_001374445.1:p.Asn94Ser, NP_001374445.1:p.Asn94Thr, NP_001374409.1:p.Asn112Ser, NP_001374409.1:p.Asn112Thr, NP_001374399.1:p.Asn112Ser, NP_001374399.1:p.Asn112Thr, NP_001374401.1:p.Asn112Ser, NP_001374401.1:p.Asn112Thr, NP_001374404.1:p.Asn112Ser, NP_001374404.1:p.Asn112Thr, NP_001374415.1:p.Asn112Ser, NP_001374415.1:p.Asn112Thr, NP_001374411.1:p.Asn112Ser, NP_001374411.1:p.Asn112Thr, NP_001374410.1:p.Asn112Ser, NP_001374410.1:p.Asn112Thr, NP_001374444.1:p.Asn112Ser, NP_001374444.1:p.Asn112Thr, NP_001374447.1:p.Asn94Ser, NP_001374447.1:p.Asn94Thr, NP_001374400.1:p.Asn112Ser, NP_001374400.1:p.Asn112Thr, NP_001374414.1:p.Asn112Ser, NP_001374414.1:p.Asn112Thr, NP_001374443.1:p.Asn112Ser, NP_001374443.1:p.Asn112Thr, NP_001374450.1:p.Asn112Ser, NP_001374450.1:p.Asn112Thr, NP_001374449.1:p.Asn112Ser, NP_001374449.1:p.Asn112Thr, NP_001374448.1:p.Asn112Ser, NP_001374448.1:p.Asn112Thr

        4.

        rs1475359772 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G [Show Flanks]
          Chromosome:
          9:110941938 (GRCh38)
          9:113704218 (GRCh37)
          Canonical SPDI:
          NC_000009.12:110941937:A:G
          Gene:
          LPAR1 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          G=0./0 (ALFA)
          G=0.000004/1 (TOPMED)
          G=0.000142/2 (TOMMO)
          HGVS:
          NC_000009.12:g.110941938A>G, NC_000009.11:g.113704218A>G, NM_001401.5:c.276T>C, NM_001401.4:c.276T>C, NM_001401.3:c.276T>C, NM_057159.4:c.276T>C, NM_057159.3:c.276T>C, NM_057159.2:c.276T>C, NM_001351410.2:c.276T>C, NM_001351410.1:c.276T>C, NM_001351409.2:c.276T>C, NM_001351409.1:c.276T>C, NM_001351407.2:c.276T>C, NM_001351407.1:c.276T>C, NM_001351413.2:c.276T>C, NM_001351413.1:c.276T>C, NM_001351412.2:c.276T>C, NM_001351412.1:c.276T>C, NM_001351408.2:c.276T>C, NM_001351408.1:c.276T>C, NM_001351415.2:c.276T>C, NM_001351415.1:c.276T>C, NM_001351418.2:c.276T>C, NM_001351418.1:c.276T>C, NM_001351414.2:c.276T>C, NM_001351414.1:c.276T>C, NM_001351416.2:c.276T>C, NM_001351416.1:c.276T>C, NM_001351411.2:c.276T>C, NM_001351411.1:c.276T>C, NM_001351417.2:c.276T>C, NM_001351417.1:c.276T>C, NM_001351398.2:c.276T>C, NM_001351398.1:c.276T>C, NM_001351401.2:c.276T>C, NM_001351401.1:c.276T>C, NM_001351406.2:c.276T>C, NM_001351406.1:c.276T>C, NM_001351400.2:c.276T>C, NM_001351400.1:c.276T>C, NM_001351420.2:c.276T>C, NM_001351420.1:c.276T>C, NM_001351399.2:c.276T>C, NM_001351399.1:c.276T>C, NM_001351402.2:c.276T>C, NM_001351402.1:c.276T>C, NM_001351419.2:c.276T>C, NM_001351419.1:c.276T>C, NM_001351405.2:c.276T>C, NM_001351405.1:c.276T>C, NM_001351404.2:c.276T>C, NM_001351404.1:c.276T>C, NM_001351397.2:c.276T>C, NM_001351397.1:c.276T>C, NM_001351403.2:c.276T>C, NM_001351403.1:c.276T>C, NM_001387494.1:c.276T>C, NM_001387490.1:c.276T>C, NM_001387492.1:c.276T>C, NM_001387501.1:c.276T>C, NM_001387498.1:c.276T>C, NM_001387512.1:c.276T>C, NM_001387513.1:c.276T>C, NM_001387505.1:c.276T>C, NM_001387489.1:c.276T>C, NM_001387508.1:c.276T>C, NM_001387495.1:c.276T>C, NM_001387509.1:c.276T>C, NM_001387517.1:c.222T>C, NM_001387496.1:c.276T>C, NM_001387484.1:c.276T>C, NM_001387491.1:c.276T>C, NM_001387507.1:c.276T>C, NM_001387506.1:c.276T>C, NM_001387473.1:c.276T>C, XM_047422903.1:c.276T>C, NM_001387511.1:c.276T>C, NM_001387487.1:c.276T>C, NM_001387479.1:c.276T>C, NM_001387483.1:c.276T>C, NM_001387474.1:c.276T>C, NM_001387502.1:c.276T>C, NM_001387510.1:c.276T>C, NM_001387504.1:c.276T>C, NM_001387478.1:c.276T>C, NM_001387488.1:c.276T>C, NM_001387493.1:c.276T>C, NM_001387476.1:c.276T>C, NM_001387477.1:c.276T>C, NM_001387503.1:c.276T>C, NM_001387497.1:c.276T>C, NM_001387516.1:c.222T>C, NM_001387480.1:c.276T>C, NM_001387470.1:c.276T>C, NM_001387472.1:c.276T>C, NM_001387475.1:c.276T>C, NM_001387486.1:c.276T>C, NM_001387482.1:c.276T>C, NM_001387481.1:c.276T>C, NM_001387515.1:c.276T>C, NM_001387518.1:c.222T>C, NM_001387471.1:c.276T>C, NM_001387485.1:c.276T>C, NM_001387514.1:c.276T>C, NM_001387521.1:c.276T>C, NM_001387520.1:c.276T>C, NM_001387519.1:c.276T>C

          5.

          rs1469943077 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            9:110942146 (GRCh38)
            9:113704426 (GRCh37)
            Canonical SPDI:
            NC_000009.12:110942145:T:C
            Gene:
            LPAR1 (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            C=0./0 (ALFA)
            C=0.000004/1 (TOPMED)
            C=0.000007/1 (GnomAD)
            HGVS:
            NC_000009.12:g.110942146T>C, NC_000009.11:g.113704426T>C, NM_001401.5:c.68A>G, NM_001401.4:c.68A>G, NM_001401.3:c.68A>G, NM_057159.4:c.68A>G, NM_057159.3:c.68A>G, NM_057159.2:c.68A>G, NM_001351410.2:c.68A>G, NM_001351410.1:c.68A>G, NM_001351409.2:c.68A>G, NM_001351409.1:c.68A>G, NM_001351407.2:c.68A>G, NM_001351407.1:c.68A>G, NM_001351413.2:c.68A>G, NM_001351413.1:c.68A>G, NM_001351412.2:c.68A>G, NM_001351412.1:c.68A>G, NM_001351408.2:c.68A>G, NM_001351408.1:c.68A>G, NM_001351415.2:c.68A>G, NM_001351415.1:c.68A>G, NM_001351418.2:c.68A>G, NM_001351418.1:c.68A>G, NM_001351414.2:c.68A>G, NM_001351414.1:c.68A>G, NM_001351416.2:c.68A>G, NM_001351416.1:c.68A>G, NM_001351411.2:c.68A>G, NM_001351411.1:c.68A>G, NM_001351417.2:c.68A>G, NM_001351417.1:c.68A>G, NM_001351398.2:c.68A>G, NM_001351398.1:c.68A>G, NM_001351401.2:c.68A>G, NM_001351401.1:c.68A>G, NM_001351406.2:c.68A>G, NM_001351406.1:c.68A>G, NM_001351400.2:c.68A>G, NM_001351400.1:c.68A>G, NM_001351420.2:c.68A>G, NM_001351420.1:c.68A>G, NM_001351399.2:c.68A>G, NM_001351399.1:c.68A>G, NM_001351402.2:c.68A>G, NM_001351402.1:c.68A>G, NM_001351419.2:c.68A>G, NM_001351419.1:c.68A>G, NM_001351405.2:c.68A>G, NM_001351405.1:c.68A>G, NM_001351404.2:c.68A>G, NM_001351404.1:c.68A>G, NM_001351397.2:c.68A>G, NM_001351397.1:c.68A>G, NM_001351403.2:c.68A>G, NM_001351403.1:c.68A>G, NM_001387494.1:c.68A>G, NM_001387490.1:c.68A>G, NM_001387492.1:c.68A>G, NM_001387501.1:c.68A>G, NM_001387498.1:c.68A>G, NM_001387512.1:c.68A>G, NM_001387513.1:c.68A>G, NM_001387505.1:c.68A>G, NM_001387489.1:c.68A>G, NM_001387508.1:c.68A>G, NM_001387495.1:c.68A>G, NM_001387509.1:c.68A>G, NM_001387517.1:c.14A>G, NM_001387496.1:c.68A>G, NM_001387484.1:c.68A>G, NM_001387491.1:c.68A>G, NM_001387507.1:c.68A>G, NM_001387506.1:c.68A>G, NM_001387473.1:c.68A>G, XM_047422903.1:c.68A>G, NM_001387511.1:c.68A>G, NM_001387487.1:c.68A>G, NM_001387479.1:c.68A>G, NM_001387483.1:c.68A>G, NM_001387474.1:c.68A>G, NM_001387502.1:c.68A>G, NM_001387510.1:c.68A>G, NM_001387504.1:c.68A>G, NM_001387478.1:c.68A>G, NM_001387488.1:c.68A>G, NM_001387493.1:c.68A>G, NM_001387476.1:c.68A>G, NM_001387477.1:c.68A>G, NM_001387503.1:c.68A>G, NM_001387497.1:c.68A>G, NM_001387516.1:c.14A>G, NM_001387480.1:c.68A>G, NM_001387470.1:c.68A>G, NM_001387472.1:c.68A>G, NM_001387475.1:c.68A>G, NM_001387486.1:c.68A>G, NM_001387482.1:c.68A>G, NM_001387481.1:c.68A>G, NM_001387515.1:c.68A>G, NM_001387518.1:c.14A>G, NM_001387471.1:c.68A>G, NM_001387485.1:c.68A>G, NM_001387514.1:c.68A>G, NM_001387521.1:c.68A>G, NM_001387520.1:c.68A>G, NM_001387519.1:c.68A>G, NP_001392.2:p.Gln23Arg, NP_476500.1:p.Gln23Arg, NP_001338339.1:p.Gln23Arg, NP_001338338.1:p.Gln23Arg, NP_001338336.1:p.Gln23Arg, NP_001338342.1:p.Gln23Arg, NP_001338341.1:p.Gln23Arg, NP_001338337.1:p.Gln23Arg, NP_001338344.1:p.Gln23Arg, NP_001338347.1:p.Gln23Arg, NP_001338343.1:p.Gln23Arg, NP_001338345.1:p.Gln23Arg, NP_001338340.1:p.Gln23Arg, NP_001338346.1:p.Gln23Arg, NP_001338327.1:p.Gln23Arg, NP_001338330.1:p.Gln23Arg, NP_001338335.1:p.Gln23Arg, NP_001338329.1:p.Gln23Arg, NP_001338349.1:p.Gln23Arg, NP_001338328.1:p.Gln23Arg, NP_001338331.1:p.Gln23Arg, NP_001338348.1:p.Gln23Arg, NP_001338334.1:p.Gln23Arg, NP_001338333.1:p.Gln23Arg, NP_001338326.1:p.Gln23Arg, NP_001338332.1:p.Gln23Arg, NP_001374423.1:p.Gln23Arg, NP_001374419.1:p.Gln23Arg, NP_001374421.1:p.Gln23Arg, NP_001374430.1:p.Gln23Arg, NP_001374427.1:p.Gln23Arg, NP_001374441.1:p.Gln23Arg, NP_001374442.1:p.Gln23Arg, NP_001374434.1:p.Gln23Arg, NP_001374418.1:p.Gln23Arg, NP_001374437.1:p.Gln23Arg, NP_001374424.1:p.Gln23Arg, NP_001374438.1:p.Gln23Arg, NP_001374446.1:p.Gln5Arg, NP_001374425.1:p.Gln23Arg, NP_001374413.1:p.Gln23Arg, NP_001374420.1:p.Gln23Arg, NP_001374436.1:p.Gln23Arg, NP_001374435.1:p.Gln23Arg, NP_001374402.1:p.Gln23Arg, XP_047278859.1:p.Gln23Arg, NP_001374440.1:p.Gln23Arg, NP_001374416.1:p.Gln23Arg, NP_001374408.1:p.Gln23Arg, NP_001374412.1:p.Gln23Arg, NP_001374403.1:p.Gln23Arg, NP_001374431.1:p.Gln23Arg, NP_001374439.1:p.Gln23Arg, NP_001374433.1:p.Gln23Arg, NP_001374407.1:p.Gln23Arg, NP_001374417.1:p.Gln23Arg, NP_001374422.1:p.Gln23Arg, NP_001374405.1:p.Gln23Arg, NP_001374406.1:p.Gln23Arg, NP_001374432.1:p.Gln23Arg, NP_001374426.1:p.Gln23Arg, NP_001374445.1:p.Gln5Arg, NP_001374409.1:p.Gln23Arg, NP_001374399.1:p.Gln23Arg, NP_001374401.1:p.Gln23Arg, NP_001374404.1:p.Gln23Arg, NP_001374415.1:p.Gln23Arg, NP_001374411.1:p.Gln23Arg, NP_001374410.1:p.Gln23Arg, NP_001374444.1:p.Gln23Arg, NP_001374447.1:p.Gln5Arg, NP_001374400.1:p.Gln23Arg, NP_001374414.1:p.Gln23Arg, NP_001374443.1:p.Gln23Arg, NP_001374450.1:p.Gln23Arg, NP_001374449.1:p.Gln23Arg, NP_001374448.1:p.Gln23Arg

            6.

            rs1468653721 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              9:110941759 (GRCh38)
              9:113704039 (GRCh37)
              Canonical SPDI:
              NC_000009.12:110941758:C:T
              Gene:
              LPAR1 (Varview)
              Functional Consequence:
              coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0.000007/1 (GnomAD)
              T=0.000008/2 (GnomAD_exomes)
              T=0.000015/4 (TOPMED)
              HGVS:
              NC_000009.12:g.110941759C>T, NC_000009.11:g.113704039C>T, NM_001401.5:c.455G>A, NM_001401.4:c.455G>A, NM_001401.3:c.455G>A, NM_057159.4:c.455G>A, NM_057159.3:c.455G>A, NM_057159.2:c.455G>A, NM_001351410.2:c.455G>A, NM_001351410.1:c.455G>A, NM_001351409.2:c.455G>A, NM_001351409.1:c.455G>A, NM_001351407.2:c.455G>A, NM_001351407.1:c.455G>A, NM_001351413.2:c.455G>A, NM_001351413.1:c.455G>A, NM_001351412.2:c.455G>A, NM_001351412.1:c.455G>A, NM_001351408.2:c.455G>A, NM_001351408.1:c.455G>A, NM_001351415.2:c.455G>A, NM_001351415.1:c.455G>A, NM_001351418.2:c.455G>A, NM_001351418.1:c.455G>A, NM_001351414.2:c.455G>A, NM_001351414.1:c.455G>A, NM_001351416.2:c.455G>A, NM_001351416.1:c.455G>A, NM_001351411.2:c.455G>A, NM_001351411.1:c.455G>A, NM_001351417.2:c.455G>A, NM_001351417.1:c.455G>A, NM_001351398.2:c.455G>A, NM_001351398.1:c.455G>A, NM_001351401.2:c.455G>A, NM_001351401.1:c.455G>A, NM_001351406.2:c.455G>A, NM_001351406.1:c.455G>A, NM_001351400.2:c.455G>A, NM_001351400.1:c.455G>A, NM_001351420.2:c.455G>A, NM_001351420.1:c.455G>A, NM_001351399.2:c.455G>A, NM_001351399.1:c.455G>A, NM_001351402.2:c.455G>A, NM_001351402.1:c.455G>A, NM_001351419.2:c.455G>A, NM_001351419.1:c.455G>A, NM_001351405.2:c.455G>A, NM_001351405.1:c.455G>A, NM_001351404.2:c.455G>A, NM_001351404.1:c.455G>A, NM_001351397.2:c.455G>A, NM_001351397.1:c.455G>A, NM_001351403.2:c.455G>A, NM_001351403.1:c.455G>A, NM_001387494.1:c.455G>A, NM_001387490.1:c.455G>A, NM_001387492.1:c.455G>A, NM_001387501.1:c.455G>A, NM_001387498.1:c.455G>A, NM_001387512.1:c.455G>A, NM_001387513.1:c.455G>A, NM_001387505.1:c.455G>A, NM_001387489.1:c.455G>A, NM_001387508.1:c.455G>A, NM_001387495.1:c.455G>A, NM_001387509.1:c.455G>A, NM_001387517.1:c.401G>A, NM_001387496.1:c.455G>A, NM_001387484.1:c.455G>A, NM_001387491.1:c.455G>A, NM_001387507.1:c.455G>A, NM_001387506.1:c.455G>A, NM_001387473.1:c.455G>A, XM_047422903.1:c.455G>A, NM_001387511.1:c.455G>A, NM_001387487.1:c.455G>A, NM_001387479.1:c.455G>A, NM_001387483.1:c.455G>A, NM_001387474.1:c.455G>A, NM_001387502.1:c.455G>A, NM_001387510.1:c.455G>A, NM_001387504.1:c.455G>A, NM_001387478.1:c.455G>A, NM_001387488.1:c.455G>A, NM_001387493.1:c.455G>A, NM_001387476.1:c.455G>A, NM_001387477.1:c.455G>A, NM_001387503.1:c.455G>A, NM_001387497.1:c.455G>A, NM_001387516.1:c.401G>A, NM_001387480.1:c.455G>A, NM_001387470.1:c.455G>A, NM_001387472.1:c.455G>A, NM_001387475.1:c.455G>A, NM_001387486.1:c.455G>A, NM_001387482.1:c.455G>A, NM_001387481.1:c.455G>A, NM_001387515.1:c.455G>A, NM_001387518.1:c.401G>A, NM_001387471.1:c.455G>A, NM_001387485.1:c.455G>A, NM_001387514.1:c.455G>A, NM_001387521.1:c.455G>A, NM_001387520.1:c.455G>A, NM_001387519.1:c.455G>A, NP_001392.2:p.Arg152His, NP_476500.1:p.Arg152His, NP_001338339.1:p.Arg152His, NP_001338338.1:p.Arg152His, NP_001338336.1:p.Arg152His, NP_001338342.1:p.Arg152His, NP_001338341.1:p.Arg152His, NP_001338337.1:p.Arg152His, NP_001338344.1:p.Arg152His, NP_001338347.1:p.Arg152His, NP_001338343.1:p.Arg152His, NP_001338345.1:p.Arg152His, NP_001338340.1:p.Arg152His, NP_001338346.1:p.Arg152His, NP_001338327.1:p.Arg152His, NP_001338330.1:p.Arg152His, NP_001338335.1:p.Arg152His, NP_001338329.1:p.Arg152His, NP_001338349.1:p.Arg152His, NP_001338328.1:p.Arg152His, NP_001338331.1:p.Arg152His, NP_001338348.1:p.Arg152His, NP_001338334.1:p.Arg152His, NP_001338333.1:p.Arg152His, NP_001338326.1:p.Arg152His, NP_001338332.1:p.Arg152His, NP_001374423.1:p.Arg152His, NP_001374419.1:p.Arg152His, NP_001374421.1:p.Arg152His, NP_001374430.1:p.Arg152His, NP_001374427.1:p.Arg152His, NP_001374441.1:p.Arg152His, NP_001374442.1:p.Arg152His, NP_001374434.1:p.Arg152His, NP_001374418.1:p.Arg152His, NP_001374437.1:p.Arg152His, NP_001374424.1:p.Arg152His, NP_001374438.1:p.Arg152His, NP_001374446.1:p.Arg134His, NP_001374425.1:p.Arg152His, NP_001374413.1:p.Arg152His, NP_001374420.1:p.Arg152His, NP_001374436.1:p.Arg152His, NP_001374435.1:p.Arg152His, NP_001374402.1:p.Arg152His, XP_047278859.1:p.Arg152His, NP_001374440.1:p.Arg152His, NP_001374416.1:p.Arg152His, NP_001374408.1:p.Arg152His, NP_001374412.1:p.Arg152His, NP_001374403.1:p.Arg152His, NP_001374431.1:p.Arg152His, NP_001374439.1:p.Arg152His, NP_001374433.1:p.Arg152His, NP_001374407.1:p.Arg152His, NP_001374417.1:p.Arg152His, NP_001374422.1:p.Arg152His, NP_001374405.1:p.Arg152His, NP_001374406.1:p.Arg152His, NP_001374432.1:p.Arg152His, NP_001374426.1:p.Arg152His, NP_001374445.1:p.Arg134His, NP_001374409.1:p.Arg152His, NP_001374399.1:p.Arg152His, NP_001374401.1:p.Arg152His, NP_001374404.1:p.Arg152His, NP_001374415.1:p.Arg152His, NP_001374411.1:p.Arg152His, NP_001374410.1:p.Arg152His, NP_001374444.1:p.Arg152His, NP_001374447.1:p.Arg134His, NP_001374400.1:p.Arg152His, NP_001374414.1:p.Arg152His, NP_001374443.1:p.Arg152His, NP_001374450.1:p.Arg152His, NP_001374449.1:p.Arg152His, NP_001374448.1:p.Arg152His

              7.

              rs1468210829 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                9:110941701 (GRCh38)
                9:113703981 (GRCh37)
                Canonical SPDI:
                NC_000009.12:110941700:G:A
                Gene:
                LPAR1 (Varview)
                Functional Consequence:
                coding_sequence_variant,synonymous_variant
                Validated:
                by frequency,by cluster
                MAF:
                A=0.0005/1 (Korea1K)
                HGVS:
                NC_000009.12:g.110941701G>A, NC_000009.11:g.113703981G>A, NM_001401.5:c.513C>T, NM_001401.4:c.513C>T, NM_001401.3:c.513C>T, NM_057159.4:c.513C>T, NM_057159.3:c.513C>T, NM_057159.2:c.513C>T, NM_001351410.2:c.513C>T, NM_001351410.1:c.513C>T, NM_001351409.2:c.513C>T, NM_001351409.1:c.513C>T, NM_001351407.2:c.513C>T, NM_001351407.1:c.513C>T, NM_001351413.2:c.513C>T, NM_001351413.1:c.513C>T, NM_001351412.2:c.513C>T, NM_001351412.1:c.513C>T, NM_001351408.2:c.513C>T, NM_001351408.1:c.513C>T, NM_001351415.2:c.513C>T, NM_001351415.1:c.513C>T, NM_001351418.2:c.513C>T, NM_001351418.1:c.513C>T, NM_001351414.2:c.513C>T, NM_001351414.1:c.513C>T, NM_001351416.2:c.513C>T, NM_001351416.1:c.513C>T, NM_001351411.2:c.513C>T, NM_001351411.1:c.513C>T, NM_001351417.2:c.513C>T, NM_001351417.1:c.513C>T, NM_001351398.2:c.513C>T, NM_001351398.1:c.513C>T, NM_001351401.2:c.513C>T, NM_001351401.1:c.513C>T, NM_001351406.2:c.513C>T, NM_001351406.1:c.513C>T, NM_001351400.2:c.513C>T, NM_001351400.1:c.513C>T, NM_001351420.2:c.513C>T, NM_001351420.1:c.513C>T, NM_001351399.2:c.513C>T, NM_001351399.1:c.513C>T, NM_001351402.2:c.513C>T, NM_001351402.1:c.513C>T, NM_001351419.2:c.513C>T, NM_001351419.1:c.513C>T, NM_001351405.2:c.513C>T, NM_001351405.1:c.513C>T, NM_001351404.2:c.513C>T, NM_001351404.1:c.513C>T, NM_001351397.2:c.513C>T, NM_001351397.1:c.513C>T, NM_001351403.2:c.513C>T, NM_001351403.1:c.513C>T, NM_001387494.1:c.513C>T, NM_001387490.1:c.513C>T, NM_001387492.1:c.513C>T, NM_001387501.1:c.513C>T, NM_001387498.1:c.513C>T, NM_001387512.1:c.513C>T, NM_001387513.1:c.513C>T, NM_001387505.1:c.513C>T, NM_001387489.1:c.513C>T, NM_001387508.1:c.513C>T, NM_001387495.1:c.513C>T, NM_001387509.1:c.513C>T, NM_001387517.1:c.459C>T, NM_001387496.1:c.513C>T, NM_001387484.1:c.513C>T, NM_001387491.1:c.513C>T, NM_001387507.1:c.513C>T, NM_001387506.1:c.513C>T, NM_001387473.1:c.513C>T, XM_047422903.1:c.513C>T, NM_001387511.1:c.513C>T, NM_001387487.1:c.513C>T, NM_001387479.1:c.513C>T, NM_001387483.1:c.513C>T, NM_001387474.1:c.513C>T, NM_001387502.1:c.513C>T, NM_001387510.1:c.513C>T, NM_001387504.1:c.513C>T, NM_001387478.1:c.513C>T, NM_001387488.1:c.513C>T, NM_001387493.1:c.513C>T, NM_001387476.1:c.513C>T, NM_001387477.1:c.513C>T, NM_001387503.1:c.513C>T, NM_001387497.1:c.513C>T, NM_001387516.1:c.459C>T, NM_001387480.1:c.513C>T, NM_001387470.1:c.513C>T, NM_001387472.1:c.513C>T, NM_001387475.1:c.513C>T, NM_001387486.1:c.513C>T, NM_001387482.1:c.513C>T, NM_001387481.1:c.513C>T, NM_001387515.1:c.513C>T, NM_001387518.1:c.459C>T, NM_001387471.1:c.513C>T, NM_001387485.1:c.513C>T, NM_001387514.1:c.513C>T, NM_001387521.1:c.513C>T, NM_001387520.1:c.513C>T, NM_001387519.1:c.513C>T

                8.

                rs1467380842 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  9:110941902 (GRCh38)
                  9:113704182 (GRCh37)
                  Canonical SPDI:
                  NC_000009.12:110941901:A:G
                  Gene:
                  LPAR1 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,synonymous_variant
                  Validated:
                  by frequency
                  MAF:
                  G=0.000004/1 (GnomAD_exomes)
                  HGVS:
                  NC_000009.12:g.110941902A>G, NC_000009.11:g.113704182A>G, NM_001401.5:c.312T>C, NM_001401.4:c.312T>C, NM_001401.3:c.312T>C, NM_057159.4:c.312T>C, NM_057159.3:c.312T>C, NM_057159.2:c.312T>C, NM_001351410.2:c.312T>C, NM_001351410.1:c.312T>C, NM_001351409.2:c.312T>C, NM_001351409.1:c.312T>C, NM_001351407.2:c.312T>C, NM_001351407.1:c.312T>C, NM_001351413.2:c.312T>C, NM_001351413.1:c.312T>C, NM_001351412.2:c.312T>C, NM_001351412.1:c.312T>C, NM_001351408.2:c.312T>C, NM_001351408.1:c.312T>C, NM_001351415.2:c.312T>C, NM_001351415.1:c.312T>C, NM_001351418.2:c.312T>C, NM_001351418.1:c.312T>C, NM_001351414.2:c.312T>C, NM_001351414.1:c.312T>C, NM_001351416.2:c.312T>C, NM_001351416.1:c.312T>C, NM_001351411.2:c.312T>C, NM_001351411.1:c.312T>C, NM_001351417.2:c.312T>C, NM_001351417.1:c.312T>C, NM_001351398.2:c.312T>C, NM_001351398.1:c.312T>C, NM_001351401.2:c.312T>C, NM_001351401.1:c.312T>C, NM_001351406.2:c.312T>C, NM_001351406.1:c.312T>C, NM_001351400.2:c.312T>C, NM_001351400.1:c.312T>C, NM_001351420.2:c.312T>C, NM_001351420.1:c.312T>C, NM_001351399.2:c.312T>C, NM_001351399.1:c.312T>C, NM_001351402.2:c.312T>C, NM_001351402.1:c.312T>C, NM_001351419.2:c.312T>C, NM_001351419.1:c.312T>C, NM_001351405.2:c.312T>C, NM_001351405.1:c.312T>C, NM_001351404.2:c.312T>C, NM_001351404.1:c.312T>C, NM_001351397.2:c.312T>C, NM_001351397.1:c.312T>C, NM_001351403.2:c.312T>C, NM_001351403.1:c.312T>C, NM_001387494.1:c.312T>C, NM_001387490.1:c.312T>C, NM_001387492.1:c.312T>C, NM_001387501.1:c.312T>C, NM_001387498.1:c.312T>C, NM_001387512.1:c.312T>C, NM_001387513.1:c.312T>C, NM_001387505.1:c.312T>C, NM_001387489.1:c.312T>C, NM_001387508.1:c.312T>C, NM_001387495.1:c.312T>C, NM_001387509.1:c.312T>C, NM_001387517.1:c.258T>C, NM_001387496.1:c.312T>C, NM_001387484.1:c.312T>C, NM_001387491.1:c.312T>C, NM_001387507.1:c.312T>C, NM_001387506.1:c.312T>C, NM_001387473.1:c.312T>C, XM_047422903.1:c.312T>C, NM_001387511.1:c.312T>C, NM_001387487.1:c.312T>C, NM_001387479.1:c.312T>C, NM_001387483.1:c.312T>C, NM_001387474.1:c.312T>C, NM_001387502.1:c.312T>C, NM_001387510.1:c.312T>C, NM_001387504.1:c.312T>C, NM_001387478.1:c.312T>C, NM_001387488.1:c.312T>C, NM_001387493.1:c.312T>C, NM_001387476.1:c.312T>C, NM_001387477.1:c.312T>C, NM_001387503.1:c.312T>C, NM_001387497.1:c.312T>C, NM_001387516.1:c.258T>C, NM_001387480.1:c.312T>C, NM_001387470.1:c.312T>C, NM_001387472.1:c.312T>C, NM_001387475.1:c.312T>C, NM_001387486.1:c.312T>C, NM_001387482.1:c.312T>C, NM_001387481.1:c.312T>C, NM_001387515.1:c.312T>C, NM_001387518.1:c.258T>C, NM_001387471.1:c.312T>C, NM_001387485.1:c.312T>C, NM_001387514.1:c.312T>C, NM_001387521.1:c.312T>C, NM_001387520.1:c.312T>C, NM_001387519.1:c.312T>C

                  9.

                  rs1466452070 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>T [Show Flanks]
                    Chromosome:
                    9:110942164 (GRCh38)
                    9:113704444 (GRCh37)
                    Canonical SPDI:
                    NC_000009.12:110942163:G:T
                    Gene:
                    LPAR1 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,intron_variant,missense_variant
                    Validated:
                    by frequency
                    MAF:
                    T=0.000008/2 (GnomAD_exomes)
                    HGVS:
                    NC_000009.12:g.110942164G>T, NC_000009.11:g.113704444G>T, NM_001401.5:c.50C>A, NM_001401.4:c.50C>A, NM_001401.3:c.50C>A, NM_057159.4:c.50C>A, NM_057159.3:c.50C>A, NM_057159.2:c.50C>A, NM_001351410.2:c.50C>A, NM_001351410.1:c.50C>A, NM_001351409.2:c.50C>A, NM_001351409.1:c.50C>A, NM_001351407.2:c.50C>A, NM_001351407.1:c.50C>A, NM_001351413.2:c.50C>A, NM_001351413.1:c.50C>A, NM_001351412.2:c.50C>A, NM_001351412.1:c.50C>A, NM_001351408.2:c.50C>A, NM_001351408.1:c.50C>A, NM_001351415.2:c.50C>A, NM_001351415.1:c.50C>A, NM_001351418.2:c.50C>A, NM_001351418.1:c.50C>A, NM_001351414.2:c.50C>A, NM_001351414.1:c.50C>A, NM_001351416.2:c.50C>A, NM_001351416.1:c.50C>A, NM_001351411.2:c.50C>A, NM_001351411.1:c.50C>A, NM_001351417.2:c.50C>A, NM_001351417.1:c.50C>A, NM_001351398.2:c.50C>A, NM_001351398.1:c.50C>A, NM_001351401.2:c.50C>A, NM_001351401.1:c.50C>A, NM_001351406.2:c.50C>A, NM_001351406.1:c.50C>A, NM_001351400.2:c.50C>A, NM_001351400.1:c.50C>A, NM_001351420.2:c.50C>A, NM_001351420.1:c.50C>A, NM_001351399.2:c.50C>A, NM_001351399.1:c.50C>A, NM_001351402.2:c.50C>A, NM_001351402.1:c.50C>A, NM_001351419.2:c.50C>A, NM_001351419.1:c.50C>A, NM_001351405.2:c.50C>A, NM_001351405.1:c.50C>A, NM_001351404.2:c.50C>A, NM_001351404.1:c.50C>A, NM_001351397.2:c.50C>A, NM_001351397.1:c.50C>A, NM_001351403.2:c.50C>A, NM_001351403.1:c.50C>A, NM_001387494.1:c.50C>A, NM_001387490.1:c.50C>A, NM_001387492.1:c.50C>A, NM_001387501.1:c.50C>A, NM_001387498.1:c.50C>A, NM_001387512.1:c.50C>A, NM_001387513.1:c.50C>A, NM_001387505.1:c.50C>A, NM_001387489.1:c.50C>A, NM_001387508.1:c.50C>A, NM_001387495.1:c.50C>A, NM_001387509.1:c.50C>A, NM_001387496.1:c.50C>A, NM_001387484.1:c.50C>A, NM_001387491.1:c.50C>A, NM_001387507.1:c.50C>A, NM_001387506.1:c.50C>A, NM_001387473.1:c.50C>A, XM_047422903.1:c.50C>A, NM_001387511.1:c.50C>A, NM_001387487.1:c.50C>A, NM_001387479.1:c.50C>A, NM_001387483.1:c.50C>A, NM_001387474.1:c.50C>A, NM_001387502.1:c.50C>A, NM_001387510.1:c.50C>A, NM_001387504.1:c.50C>A, NM_001387478.1:c.50C>A, NM_001387488.1:c.50C>A, NM_001387493.1:c.50C>A, NM_001387476.1:c.50C>A, NM_001387477.1:c.50C>A, NM_001387503.1:c.50C>A, NM_001387497.1:c.50C>A, NM_001387480.1:c.50C>A, NM_001387470.1:c.50C>A, NM_001387472.1:c.50C>A, NM_001387475.1:c.50C>A, NM_001387486.1:c.50C>A, NM_001387482.1:c.50C>A, NM_001387481.1:c.50C>A, NM_001387515.1:c.50C>A, NM_001387471.1:c.50C>A, NM_001387485.1:c.50C>A, NM_001387514.1:c.50C>A, NM_001387521.1:c.50C>A, NM_001387520.1:c.50C>A, NM_001387519.1:c.50C>A, NP_001392.2:p.Thr17Lys, NP_476500.1:p.Thr17Lys, NP_001338339.1:p.Thr17Lys, NP_001338338.1:p.Thr17Lys, NP_001338336.1:p.Thr17Lys, NP_001338342.1:p.Thr17Lys, NP_001338341.1:p.Thr17Lys, NP_001338337.1:p.Thr17Lys, NP_001338344.1:p.Thr17Lys, NP_001338347.1:p.Thr17Lys, NP_001338343.1:p.Thr17Lys, NP_001338345.1:p.Thr17Lys, NP_001338340.1:p.Thr17Lys, NP_001338346.1:p.Thr17Lys, NP_001338327.1:p.Thr17Lys, NP_001338330.1:p.Thr17Lys, NP_001338335.1:p.Thr17Lys, NP_001338329.1:p.Thr17Lys, NP_001338349.1:p.Thr17Lys, NP_001338328.1:p.Thr17Lys, NP_001338331.1:p.Thr17Lys, NP_001338348.1:p.Thr17Lys, NP_001338334.1:p.Thr17Lys, NP_001338333.1:p.Thr17Lys, NP_001338326.1:p.Thr17Lys, NP_001338332.1:p.Thr17Lys, NP_001374423.1:p.Thr17Lys, NP_001374419.1:p.Thr17Lys, NP_001374421.1:p.Thr17Lys, NP_001374430.1:p.Thr17Lys, NP_001374427.1:p.Thr17Lys, NP_001374441.1:p.Thr17Lys, NP_001374442.1:p.Thr17Lys, NP_001374434.1:p.Thr17Lys, NP_001374418.1:p.Thr17Lys, NP_001374437.1:p.Thr17Lys, NP_001374424.1:p.Thr17Lys, NP_001374438.1:p.Thr17Lys, NP_001374425.1:p.Thr17Lys, NP_001374413.1:p.Thr17Lys, NP_001374420.1:p.Thr17Lys, NP_001374436.1:p.Thr17Lys, NP_001374435.1:p.Thr17Lys, NP_001374402.1:p.Thr17Lys, XP_047278859.1:p.Thr17Lys, NP_001374440.1:p.Thr17Lys, NP_001374416.1:p.Thr17Lys, NP_001374408.1:p.Thr17Lys, NP_001374412.1:p.Thr17Lys, NP_001374403.1:p.Thr17Lys, NP_001374431.1:p.Thr17Lys, NP_001374439.1:p.Thr17Lys, NP_001374433.1:p.Thr17Lys, NP_001374407.1:p.Thr17Lys, NP_001374417.1:p.Thr17Lys, NP_001374422.1:p.Thr17Lys, NP_001374405.1:p.Thr17Lys, NP_001374406.1:p.Thr17Lys, NP_001374432.1:p.Thr17Lys, NP_001374426.1:p.Thr17Lys, NP_001374409.1:p.Thr17Lys, NP_001374399.1:p.Thr17Lys, NP_001374401.1:p.Thr17Lys, NP_001374404.1:p.Thr17Lys, NP_001374415.1:p.Thr17Lys, NP_001374411.1:p.Thr17Lys, NP_001374410.1:p.Thr17Lys, NP_001374444.1:p.Thr17Lys, NP_001374400.1:p.Thr17Lys, NP_001374414.1:p.Thr17Lys, NP_001374443.1:p.Thr17Lys, NP_001374450.1:p.Thr17Lys, NP_001374449.1:p.Thr17Lys, NP_001374448.1:p.Thr17Lys

                    10.

                    rs1464620103 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>A [Show Flanks]
                      Chromosome:
                      9:110941624 (GRCh38)
                      9:113703904 (GRCh37)
                      Canonical SPDI:
                      NC_000009.12:110941623:T:A
                      Gene:
                      LPAR1 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant
                      HGVS:
                      NC_000009.12:g.110941624T>A, NC_000009.11:g.113703904T>A, NM_001401.5:c.590A>T, NM_001401.4:c.590A>T, NM_001401.3:c.590A>T, NM_057159.4:c.590A>T, NM_057159.3:c.590A>T, NM_057159.2:c.590A>T, NM_001351410.2:c.590A>T, NM_001351410.1:c.590A>T, NM_001351409.2:c.590A>T, NM_001351409.1:c.590A>T, NM_001351407.2:c.590A>T, NM_001351407.1:c.590A>T, NM_001351413.2:c.590A>T, NM_001351413.1:c.590A>T, NM_001351412.2:c.590A>T, NM_001351412.1:c.590A>T, NM_001351408.2:c.590A>T, NM_001351408.1:c.590A>T, NM_001351415.2:c.590A>T, NM_001351415.1:c.590A>T, NM_001351418.2:c.590A>T, NM_001351418.1:c.590A>T, NM_001351414.2:c.590A>T, NM_001351414.1:c.590A>T, NM_001351416.2:c.590A>T, NM_001351416.1:c.590A>T, NM_001351411.2:c.590A>T, NM_001351411.1:c.590A>T, NM_001351417.2:c.590A>T, NM_001351417.1:c.590A>T, NM_001351398.2:c.590A>T, NM_001351398.1:c.590A>T, NM_001351401.2:c.590A>T, NM_001351401.1:c.590A>T, NM_001351406.2:c.590A>T, NM_001351406.1:c.590A>T, NM_001351400.2:c.590A>T, NM_001351400.1:c.590A>T, NM_001351420.2:c.590A>T, NM_001351420.1:c.590A>T, NM_001351399.2:c.590A>T, NM_001351399.1:c.590A>T, NM_001351402.2:c.590A>T, NM_001351402.1:c.590A>T, NM_001351419.2:c.590A>T, NM_001351419.1:c.590A>T, NM_001351405.2:c.590A>T, NM_001351405.1:c.590A>T, NM_001351404.2:c.590A>T, NM_001351404.1:c.590A>T, NM_001351397.2:c.590A>T, NM_001351397.1:c.590A>T, NM_001351403.2:c.590A>T, NM_001351403.1:c.590A>T, NM_001387494.1:c.590A>T, NM_001387490.1:c.590A>T, NM_001387492.1:c.590A>T, NM_001387501.1:c.590A>T, NM_001387498.1:c.590A>T, NM_001387512.1:c.590A>T, NM_001387513.1:c.590A>T, NM_001387505.1:c.590A>T, NM_001387489.1:c.590A>T, NM_001387508.1:c.590A>T, NM_001387495.1:c.590A>T, NM_001387509.1:c.590A>T, NM_001387517.1:c.536A>T, NM_001387496.1:c.590A>T, NM_001387484.1:c.590A>T, NM_001387491.1:c.590A>T, NM_001387507.1:c.590A>T, NM_001387506.1:c.590A>T, NM_001387473.1:c.590A>T, XM_047422903.1:c.590A>T, NM_001387511.1:c.590A>T, NM_001387487.1:c.590A>T, NM_001387479.1:c.590A>T, NM_001387483.1:c.590A>T, NM_001387474.1:c.590A>T, NM_001387502.1:c.590A>T, NM_001387510.1:c.590A>T, NM_001387504.1:c.590A>T, NM_001387478.1:c.590A>T, NM_001387488.1:c.590A>T, NM_001387493.1:c.590A>T, NM_001387476.1:c.590A>T, NM_001387477.1:c.590A>T, NM_001387503.1:c.590A>T, NM_001387497.1:c.590A>T, NM_001387516.1:c.536A>T, NM_001387480.1:c.590A>T, NM_001387470.1:c.590A>T, NM_001387472.1:c.590A>T, NM_001387475.1:c.590A>T, NM_001387486.1:c.590A>T, NM_001387482.1:c.590A>T, NM_001387481.1:c.590A>T, NM_001387515.1:c.590A>T, NM_001387518.1:c.536A>T, NM_001387471.1:c.590A>T, NM_001387485.1:c.590A>T, NM_001387514.1:c.590A>T, NM_001387521.1:c.590A>T, NM_001387520.1:c.590A>T, NM_001387519.1:c.590A>T, NP_001392.2:p.Asn197Ile, NP_476500.1:p.Asn197Ile, NP_001338339.1:p.Asn197Ile, NP_001338338.1:p.Asn197Ile, NP_001338336.1:p.Asn197Ile, NP_001338342.1:p.Asn197Ile, NP_001338341.1:p.Asn197Ile, NP_001338337.1:p.Asn197Ile, NP_001338344.1:p.Asn197Ile, NP_001338347.1:p.Asn197Ile, NP_001338343.1:p.Asn197Ile, NP_001338345.1:p.Asn197Ile, NP_001338340.1:p.Asn197Ile, NP_001338346.1:p.Asn197Ile, NP_001338327.1:p.Asn197Ile, NP_001338330.1:p.Asn197Ile, NP_001338335.1:p.Asn197Ile, NP_001338329.1:p.Asn197Ile, NP_001338349.1:p.Asn197Ile, NP_001338328.1:p.Asn197Ile, NP_001338331.1:p.Asn197Ile, NP_001338348.1:p.Asn197Ile, NP_001338334.1:p.Asn197Ile, NP_001338333.1:p.Asn197Ile, NP_001338326.1:p.Asn197Ile, NP_001338332.1:p.Asn197Ile, NP_001374423.1:p.Asn197Ile, NP_001374419.1:p.Asn197Ile, NP_001374421.1:p.Asn197Ile, NP_001374430.1:p.Asn197Ile, NP_001374427.1:p.Asn197Ile, NP_001374441.1:p.Asn197Ile, NP_001374442.1:p.Asn197Ile, NP_001374434.1:p.Asn197Ile, NP_001374418.1:p.Asn197Ile, NP_001374437.1:p.Asn197Ile, NP_001374424.1:p.Asn197Ile, NP_001374438.1:p.Asn197Ile, NP_001374446.1:p.Asn179Ile, NP_001374425.1:p.Asn197Ile, NP_001374413.1:p.Asn197Ile, NP_001374420.1:p.Asn197Ile, NP_001374436.1:p.Asn197Ile, NP_001374435.1:p.Asn197Ile, NP_001374402.1:p.Asn197Ile, XP_047278859.1:p.Asn197Ile, NP_001374440.1:p.Asn197Ile, NP_001374416.1:p.Asn197Ile, NP_001374408.1:p.Asn197Ile, NP_001374412.1:p.Asn197Ile, NP_001374403.1:p.Asn197Ile, NP_001374431.1:p.Asn197Ile, NP_001374439.1:p.Asn197Ile, NP_001374433.1:p.Asn197Ile, NP_001374407.1:p.Asn197Ile, NP_001374417.1:p.Asn197Ile, NP_001374422.1:p.Asn197Ile, NP_001374405.1:p.Asn197Ile, NP_001374406.1:p.Asn197Ile, NP_001374432.1:p.Asn197Ile, NP_001374426.1:p.Asn197Ile, NP_001374445.1:p.Asn179Ile, NP_001374409.1:p.Asn197Ile, NP_001374399.1:p.Asn197Ile, NP_001374401.1:p.Asn197Ile, NP_001374404.1:p.Asn197Ile, NP_001374415.1:p.Asn197Ile, NP_001374411.1:p.Asn197Ile, NP_001374410.1:p.Asn197Ile, NP_001374444.1:p.Asn197Ile, NP_001374447.1:p.Asn179Ile, NP_001374400.1:p.Asn197Ile, NP_001374414.1:p.Asn197Ile, NP_001374443.1:p.Asn197Ile, NP_001374450.1:p.Asn197Ile, NP_001374449.1:p.Asn197Ile, NP_001374448.1:p.Asn197Ile

                      11.

                      rs1462298664 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>A [Show Flanks]
                        Chromosome:
                        9:110875457 (GRCh38)
                        9:113637737 (GRCh37)
                        Canonical SPDI:
                        NC_000009.12:110875456:C:A
                        Gene:
                        LPAR1 (Varview)
                        Functional Consequence:
                        coding_sequence_variant,missense_variant,genic_downstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        A=0.000008/2 (TOPMED)
                        HGVS:
                        NC_000009.12:g.110875457C>A, NC_000009.11:g.113637737C>A, NM_001401.5:c.1059G>T, NM_001401.4:c.1059G>T, NM_001401.3:c.1059G>T, NM_057159.4:c.1059G>T, NM_057159.3:c.1059G>T, NM_057159.2:c.1059G>T, NM_001351410.2:c.1059G>T, NM_001351410.1:c.1059G>T, NM_001351409.2:c.1059G>T, NM_001351409.1:c.1059G>T, NM_001351407.2:c.1059G>T, NM_001351407.1:c.1059G>T, NM_001351413.2:c.1059G>T, NM_001351413.1:c.1059G>T, NM_001351412.2:c.1059G>T, NM_001351412.1:c.1059G>T, NM_001351408.2:c.1059G>T, NM_001351408.1:c.1059G>T, NM_001351415.2:c.1059G>T, NM_001351415.1:c.1059G>T, NM_001351418.2:c.1059G>T, NM_001351418.1:c.1059G>T, NM_001351414.2:c.1059G>T, NM_001351414.1:c.1059G>T, NM_001351416.2:c.1059G>T, NM_001351416.1:c.1059G>T, NM_001351411.2:c.1059G>T, NM_001351411.1:c.1059G>T, NM_001351417.2:c.1059G>T, NM_001351417.1:c.1059G>T, NM_001351398.2:c.1059G>T, NM_001351398.1:c.1059G>T, NM_001351401.2:c.1059G>T, NM_001351401.1:c.1059G>T, NM_001351406.2:c.1059G>T, NM_001351406.1:c.1059G>T, NM_001351400.2:c.1059G>T, NM_001351400.1:c.1059G>T, NM_001351420.2:c.1059G>T, NM_001351420.1:c.1059G>T, NM_001351399.2:c.1059G>T, NM_001351399.1:c.1059G>T, NM_001351402.2:c.1059G>T, NM_001351402.1:c.1059G>T, NM_001351419.2:c.1059G>T, NM_001351419.1:c.1059G>T, NM_001351405.2:c.1059G>T, NM_001351405.1:c.1059G>T, NM_001351404.2:c.1059G>T, NM_001351404.1:c.1059G>T, NM_001351397.2:c.1059G>T, NM_001351397.1:c.1059G>T, NM_001351403.2:c.1059G>T, NM_001351403.1:c.1059G>T, NM_001387494.1:c.1059G>T, NM_001387490.1:c.1059G>T, NM_001387492.1:c.1059G>T, NM_001387501.1:c.1059G>T, NM_001387498.1:c.1059G>T, NM_001387512.1:c.1059G>T, NM_001387513.1:c.1059G>T, NM_001387505.1:c.1059G>T, NM_001387489.1:c.1059G>T, NM_001387508.1:c.1059G>T, NM_001387495.1:c.1059G>T, NM_001387509.1:c.1059G>T, NM_001387517.1:c.1005G>T, NM_001387496.1:c.1059G>T, NM_001387484.1:c.1059G>T, NM_001387491.1:c.1059G>T, NM_001387507.1:c.1059G>T, NM_001387506.1:c.1059G>T, NM_001387473.1:c.1059G>T, XM_047422903.1:c.1059G>T, NM_001387511.1:c.1059G>T, NM_001387487.1:c.1059G>T, NM_001387479.1:c.1059G>T, NM_001387483.1:c.1059G>T, NM_001387474.1:c.1059G>T, NM_001387502.1:c.1059G>T, NM_001387510.1:c.1059G>T, NM_001387504.1:c.1059G>T, NM_001387478.1:c.1059G>T, NM_001387488.1:c.1059G>T, NM_001387493.1:c.1059G>T, NM_001387476.1:c.1059G>T, NM_001387477.1:c.1059G>T, NM_001387503.1:c.1059G>T, NM_001387497.1:c.1059G>T, NM_001387516.1:c.1005G>T, NM_001387480.1:c.1059G>T, NM_001387470.1:c.1059G>T, NM_001387472.1:c.1059G>T, NM_001387475.1:c.1059G>T, NM_001387486.1:c.1059G>T, NM_001387482.1:c.1059G>T, NM_001387481.1:c.1059G>T, NM_001387515.1:c.1059G>T, NM_001387518.1:c.1005G>T, NM_001387471.1:c.1059G>T, NM_001387485.1:c.1059G>T, NM_001387514.1:c.1059G>T, NP_001392.2:p.Leu353Phe, NP_476500.1:p.Leu353Phe, NP_001338339.1:p.Leu353Phe, NP_001338338.1:p.Leu353Phe, NP_001338336.1:p.Leu353Phe, NP_001338342.1:p.Leu353Phe, NP_001338341.1:p.Leu353Phe, NP_001338337.1:p.Leu353Phe, NP_001338344.1:p.Leu353Phe, NP_001338347.1:p.Leu353Phe, NP_001338343.1:p.Leu353Phe, NP_001338345.1:p.Leu353Phe, NP_001338340.1:p.Leu353Phe, NP_001338346.1:p.Leu353Phe, NP_001338327.1:p.Leu353Phe, NP_001338330.1:p.Leu353Phe, NP_001338335.1:p.Leu353Phe, NP_001338329.1:p.Leu353Phe, NP_001338349.1:p.Leu353Phe, NP_001338328.1:p.Leu353Phe, NP_001338331.1:p.Leu353Phe, NP_001338348.1:p.Leu353Phe, NP_001338334.1:p.Leu353Phe, NP_001338333.1:p.Leu353Phe, NP_001338326.1:p.Leu353Phe, NP_001338332.1:p.Leu353Phe, NP_001374423.1:p.Leu353Phe, NP_001374419.1:p.Leu353Phe, NP_001374421.1:p.Leu353Phe, NP_001374430.1:p.Leu353Phe, NP_001374427.1:p.Leu353Phe, NP_001374441.1:p.Leu353Phe, NP_001374442.1:p.Leu353Phe, NP_001374434.1:p.Leu353Phe, NP_001374418.1:p.Leu353Phe, NP_001374437.1:p.Leu353Phe, NP_001374424.1:p.Leu353Phe, NP_001374438.1:p.Leu353Phe, NP_001374446.1:p.Leu335Phe, NP_001374425.1:p.Leu353Phe, NP_001374413.1:p.Leu353Phe, NP_001374420.1:p.Leu353Phe, NP_001374436.1:p.Leu353Phe, NP_001374435.1:p.Leu353Phe, NP_001374402.1:p.Leu353Phe, XP_047278859.1:p.Leu353Phe, NP_001374440.1:p.Leu353Phe, NP_001374416.1:p.Leu353Phe, NP_001374408.1:p.Leu353Phe, NP_001374412.1:p.Leu353Phe, NP_001374403.1:p.Leu353Phe, NP_001374431.1:p.Leu353Phe, NP_001374439.1:p.Leu353Phe, NP_001374433.1:p.Leu353Phe, NP_001374407.1:p.Leu353Phe, NP_001374417.1:p.Leu353Phe, NP_001374422.1:p.Leu353Phe, NP_001374405.1:p.Leu353Phe, NP_001374406.1:p.Leu353Phe, NP_001374432.1:p.Leu353Phe, NP_001374426.1:p.Leu353Phe, NP_001374445.1:p.Leu335Phe, NP_001374409.1:p.Leu353Phe, NP_001374399.1:p.Leu353Phe, NP_001374401.1:p.Leu353Phe, NP_001374404.1:p.Leu353Phe, NP_001374415.1:p.Leu353Phe, NP_001374411.1:p.Leu353Phe, NP_001374410.1:p.Leu353Phe, NP_001374444.1:p.Leu353Phe, NP_001374447.1:p.Leu335Phe, NP_001374400.1:p.Leu353Phe, NP_001374414.1:p.Leu353Phe, NP_001374443.1:p.Leu353Phe

                        12.

                        rs1461939223 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          9:110972094 (GRCh38)
                          9:113734374 (GRCh37)
                          Canonical SPDI:
                          NC_000009.12:110972093:G:A
                          Gene:
                          LPAR1 (Varview)
                          Functional Consequence:
                          coding_sequence_variant,synonymous_variant,5_prime_UTR_variant
                          HGVS:
                          NC_000009.12:g.110972094G>A, NC_000009.11:g.113734374G>A, NM_001401.5:c.24C>T, NM_001401.4:c.24C>T, NM_001401.3:c.24C>T, NM_057159.4:c.24C>T, NM_057159.3:c.24C>T, NM_057159.2:c.24C>T, NM_001351410.2:c.24C>T, NM_001351410.1:c.24C>T, NM_001351409.2:c.24C>T, NM_001351409.1:c.24C>T, NM_001351407.2:c.24C>T, NM_001351407.1:c.24C>T, NM_001351413.2:c.24C>T, NM_001351413.1:c.24C>T, NM_001351412.2:c.24C>T, NM_001351412.1:c.24C>T, NM_001351408.2:c.24C>T, NM_001351408.1:c.24C>T, NM_001351415.2:c.24C>T, NM_001351415.1:c.24C>T, NM_001351418.2:c.24C>T, NM_001351418.1:c.24C>T, NM_001351414.2:c.24C>T, NM_001351414.1:c.24C>T, NM_001351416.2:c.24C>T, NM_001351416.1:c.24C>T, NM_001351411.2:c.24C>T, NM_001351411.1:c.24C>T, NM_001351417.2:c.24C>T, NM_001351417.1:c.24C>T, NM_001351398.2:c.24C>T, NM_001351398.1:c.24C>T, NM_001351401.2:c.24C>T, NM_001351401.1:c.24C>T, NM_001351406.2:c.24C>T, NM_001351406.1:c.24C>T, NM_001351400.2:c.24C>T, NM_001351400.1:c.24C>T, NM_001351420.2:c.24C>T, NM_001351420.1:c.24C>T, NM_001351399.2:c.24C>T, NM_001351399.1:c.24C>T, NM_001351402.2:c.24C>T, NM_001351402.1:c.24C>T, NM_001351419.2:c.24C>T, NM_001351419.1:c.24C>T, NM_001351405.2:c.24C>T, NM_001351405.1:c.24C>T, NM_001351404.2:c.24C>T, NM_001351404.1:c.24C>T, NM_001351397.2:c.24C>T, NM_001351397.1:c.24C>T, NM_001351403.2:c.24C>T, NM_001351403.1:c.24C>T, NM_001387494.1:c.24C>T, NM_001387490.1:c.24C>T, NM_001387492.1:c.24C>T, NM_001387501.1:c.24C>T, NM_001387498.1:c.24C>T, NM_001387512.1:c.24C>T, NM_001387513.1:c.24C>T, NM_001387505.1:c.24C>T, NM_001387489.1:c.24C>T, NM_001387508.1:c.24C>T, NM_001387495.1:c.24C>T, NM_001387509.1:c.24C>T, NM_001387517.1:c.-24C>T, NM_001387496.1:c.24C>T, NM_001387484.1:c.24C>T, NM_001387491.1:c.24C>T, NM_001387507.1:c.24C>T, NM_001387506.1:c.24C>T, NM_001387473.1:c.24C>T, XM_047422903.1:c.24C>T, NM_001387511.1:c.24C>T, NM_001387487.1:c.24C>T, NM_001387479.1:c.24C>T, NM_001387483.1:c.24C>T, NM_001387474.1:c.24C>T, NM_001387502.1:c.24C>T, NM_001387510.1:c.24C>T, NM_001387504.1:c.24C>T, NM_001387478.1:c.24C>T, NM_001387488.1:c.24C>T, NM_001387493.1:c.24C>T, NM_001387476.1:c.24C>T, NM_001387477.1:c.24C>T, NM_001387503.1:c.24C>T, NM_001387497.1:c.24C>T, NM_001387516.1:c.-24C>T, NM_001387480.1:c.24C>T, NM_001387470.1:c.24C>T, NM_001387472.1:c.24C>T, NM_001387475.1:c.24C>T, NM_001387486.1:c.24C>T, NM_001387482.1:c.24C>T, NM_001387481.1:c.24C>T, NM_001387515.1:c.24C>T, NM_001387518.1:c.-24C>T, NM_001387471.1:c.24C>T, NM_001387485.1:c.24C>T, NM_001387514.1:c.24C>T, NM_001387521.1:c.24C>T, NM_001387520.1:c.24C>T, NM_001387519.1:c.24C>T

                          13.

                          rs1461603368 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>G [Show Flanks]
                            Chromosome:
                            9:110942083 (GRCh38)
                            9:113704363 (GRCh37)
                            Canonical SPDI:
                            NC_000009.12:110942082:T:G
                            Gene:
                            LPAR1 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,missense_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            G=0./0 (ALFA)
                            G=0.000008/2 (TOPMED)
                            G=0.000014/2 (GnomAD)
                            HGVS:
                            NC_000009.12:g.110942083T>G, NC_000009.11:g.113704363T>G, NM_001401.5:c.131A>C, NM_001401.4:c.131A>C, NM_001401.3:c.131A>C, NM_057159.4:c.131A>C, NM_057159.3:c.131A>C, NM_057159.2:c.131A>C, NM_001351410.2:c.131A>C, NM_001351410.1:c.131A>C, NM_001351409.2:c.131A>C, NM_001351409.1:c.131A>C, NM_001351407.2:c.131A>C, NM_001351407.1:c.131A>C, NM_001351413.2:c.131A>C, NM_001351413.1:c.131A>C, NM_001351412.2:c.131A>C, NM_001351412.1:c.131A>C, NM_001351408.2:c.131A>C, NM_001351408.1:c.131A>C, NM_001351415.2:c.131A>C, NM_001351415.1:c.131A>C, NM_001351418.2:c.131A>C, NM_001351418.1:c.131A>C, NM_001351414.2:c.131A>C, NM_001351414.1:c.131A>C, NM_001351416.2:c.131A>C, NM_001351416.1:c.131A>C, NM_001351411.2:c.131A>C, NM_001351411.1:c.131A>C, NM_001351417.2:c.131A>C, NM_001351417.1:c.131A>C, NM_001351398.2:c.131A>C, NM_001351398.1:c.131A>C, NM_001351401.2:c.131A>C, NM_001351401.1:c.131A>C, NM_001351406.2:c.131A>C, NM_001351406.1:c.131A>C, NM_001351400.2:c.131A>C, NM_001351400.1:c.131A>C, NM_001351420.2:c.131A>C, NM_001351420.1:c.131A>C, NM_001351399.2:c.131A>C, NM_001351399.1:c.131A>C, NM_001351402.2:c.131A>C, NM_001351402.1:c.131A>C, NM_001351419.2:c.131A>C, NM_001351419.1:c.131A>C, NM_001351405.2:c.131A>C, NM_001351405.1:c.131A>C, NM_001351404.2:c.131A>C, NM_001351404.1:c.131A>C, NM_001351397.2:c.131A>C, NM_001351397.1:c.131A>C, NM_001351403.2:c.131A>C, NM_001351403.1:c.131A>C, NM_001387494.1:c.131A>C, NM_001387490.1:c.131A>C, NM_001387492.1:c.131A>C, NM_001387501.1:c.131A>C, NM_001387498.1:c.131A>C, NM_001387512.1:c.131A>C, NM_001387513.1:c.131A>C, NM_001387505.1:c.131A>C, NM_001387489.1:c.131A>C, NM_001387508.1:c.131A>C, NM_001387495.1:c.131A>C, NM_001387509.1:c.131A>C, NM_001387517.1:c.77A>C, NM_001387496.1:c.131A>C, NM_001387484.1:c.131A>C, NM_001387491.1:c.131A>C, NM_001387507.1:c.131A>C, NM_001387506.1:c.131A>C, NM_001387473.1:c.131A>C, XM_047422903.1:c.131A>C, NM_001387511.1:c.131A>C, NM_001387487.1:c.131A>C, NM_001387479.1:c.131A>C, NM_001387483.1:c.131A>C, NM_001387474.1:c.131A>C, NM_001387502.1:c.131A>C, NM_001387510.1:c.131A>C, NM_001387504.1:c.131A>C, NM_001387478.1:c.131A>C, NM_001387488.1:c.131A>C, NM_001387493.1:c.131A>C, NM_001387476.1:c.131A>C, NM_001387477.1:c.131A>C, NM_001387503.1:c.131A>C, NM_001387497.1:c.131A>C, NM_001387516.1:c.77A>C, NM_001387480.1:c.131A>C, NM_001387470.1:c.131A>C, NM_001387472.1:c.131A>C, NM_001387475.1:c.131A>C, NM_001387486.1:c.131A>C, NM_001387482.1:c.131A>C, NM_001387481.1:c.131A>C, NM_001387515.1:c.131A>C, NM_001387518.1:c.77A>C, NM_001387471.1:c.131A>C, NM_001387485.1:c.131A>C, NM_001387514.1:c.131A>C, NM_001387521.1:c.131A>C, NM_001387520.1:c.131A>C, NM_001387519.1:c.131A>C, NP_001392.2:p.Glu44Ala, NP_476500.1:p.Glu44Ala, NP_001338339.1:p.Glu44Ala, NP_001338338.1:p.Glu44Ala, NP_001338336.1:p.Glu44Ala, NP_001338342.1:p.Glu44Ala, NP_001338341.1:p.Glu44Ala, NP_001338337.1:p.Glu44Ala, NP_001338344.1:p.Glu44Ala, NP_001338347.1:p.Glu44Ala, NP_001338343.1:p.Glu44Ala, NP_001338345.1:p.Glu44Ala, NP_001338340.1:p.Glu44Ala, NP_001338346.1:p.Glu44Ala, NP_001338327.1:p.Glu44Ala, NP_001338330.1:p.Glu44Ala, NP_001338335.1:p.Glu44Ala, NP_001338329.1:p.Glu44Ala, NP_001338349.1:p.Glu44Ala, NP_001338328.1:p.Glu44Ala, NP_001338331.1:p.Glu44Ala, NP_001338348.1:p.Glu44Ala, NP_001338334.1:p.Glu44Ala, NP_001338333.1:p.Glu44Ala, NP_001338326.1:p.Glu44Ala, NP_001338332.1:p.Glu44Ala, NP_001374423.1:p.Glu44Ala, NP_001374419.1:p.Glu44Ala, NP_001374421.1:p.Glu44Ala, NP_001374430.1:p.Glu44Ala, NP_001374427.1:p.Glu44Ala, NP_001374441.1:p.Glu44Ala, NP_001374442.1:p.Glu44Ala, NP_001374434.1:p.Glu44Ala, NP_001374418.1:p.Glu44Ala, NP_001374437.1:p.Glu44Ala, NP_001374424.1:p.Glu44Ala, NP_001374438.1:p.Glu44Ala, NP_001374446.1:p.Glu26Ala, NP_001374425.1:p.Glu44Ala, NP_001374413.1:p.Glu44Ala, NP_001374420.1:p.Glu44Ala, NP_001374436.1:p.Glu44Ala, NP_001374435.1:p.Glu44Ala, NP_001374402.1:p.Glu44Ala, XP_047278859.1:p.Glu44Ala, NP_001374440.1:p.Glu44Ala, NP_001374416.1:p.Glu44Ala, NP_001374408.1:p.Glu44Ala, NP_001374412.1:p.Glu44Ala, NP_001374403.1:p.Glu44Ala, NP_001374431.1:p.Glu44Ala, NP_001374439.1:p.Glu44Ala, NP_001374433.1:p.Glu44Ala, NP_001374407.1:p.Glu44Ala, NP_001374417.1:p.Glu44Ala, NP_001374422.1:p.Glu44Ala, NP_001374405.1:p.Glu44Ala, NP_001374406.1:p.Glu44Ala, NP_001374432.1:p.Glu44Ala, NP_001374426.1:p.Glu44Ala, NP_001374445.1:p.Glu26Ala, NP_001374409.1:p.Glu44Ala, NP_001374399.1:p.Glu44Ala, NP_001374401.1:p.Glu44Ala, NP_001374404.1:p.Glu44Ala, NP_001374415.1:p.Glu44Ala, NP_001374411.1:p.Glu44Ala, NP_001374410.1:p.Glu44Ala, NP_001374444.1:p.Glu44Ala, NP_001374447.1:p.Glu26Ala, NP_001374400.1:p.Glu44Ala, NP_001374414.1:p.Glu44Ala, NP_001374443.1:p.Glu44Ala, NP_001374450.1:p.Glu44Ala, NP_001374449.1:p.Glu44Ala, NP_001374448.1:p.Glu44Ala

                            14.

                            rs1454983307 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              9:110875658 (GRCh38)
                              9:113637938 (GRCh37)
                              Canonical SPDI:
                              NC_000009.12:110875657:C:T
                              Gene:
                              LPAR1 (Varview)
                              Functional Consequence:
                              coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0.000028/1 (ALFA)
                              T=0.000007/1 (GnomAD)
                              T=0.000008/2 (GnomAD_exomes)
                              T=0.000008/2 (TOPMED)
                              HGVS:
                              NC_000009.12:g.110875658C>T, NC_000009.11:g.113637938C>T, NM_001401.5:c.858G>A, NM_001401.4:c.858G>A, NM_001401.3:c.858G>A, NM_057159.4:c.858G>A, NM_057159.3:c.858G>A, NM_057159.2:c.858G>A, NM_001351410.2:c.858G>A, NM_001351410.1:c.858G>A, NM_001351409.2:c.858G>A, NM_001351409.1:c.858G>A, NM_001351407.2:c.858G>A, NM_001351407.1:c.858G>A, NM_001351413.2:c.858G>A, NM_001351413.1:c.858G>A, NM_001351412.2:c.858G>A, NM_001351412.1:c.858G>A, NM_001351408.2:c.858G>A, NM_001351408.1:c.858G>A, NM_001351415.2:c.858G>A, NM_001351415.1:c.858G>A, NM_001351418.2:c.858G>A, NM_001351418.1:c.858G>A, NM_001351414.2:c.858G>A, NM_001351414.1:c.858G>A, NM_001351416.2:c.858G>A, NM_001351416.1:c.858G>A, NM_001351411.2:c.858G>A, NM_001351411.1:c.858G>A, NM_001351417.2:c.858G>A, NM_001351417.1:c.858G>A, NM_001351398.2:c.858G>A, NM_001351398.1:c.858G>A, NM_001351401.2:c.858G>A, NM_001351401.1:c.858G>A, NM_001351406.2:c.858G>A, NM_001351406.1:c.858G>A, NM_001351400.2:c.858G>A, NM_001351400.1:c.858G>A, NM_001351420.2:c.858G>A, NM_001351420.1:c.858G>A, NM_001351399.2:c.858G>A, NM_001351399.1:c.858G>A, NM_001351402.2:c.858G>A, NM_001351402.1:c.858G>A, NM_001351419.2:c.858G>A, NM_001351419.1:c.858G>A, NM_001351405.2:c.858G>A, NM_001351405.1:c.858G>A, NM_001351404.2:c.858G>A, NM_001351404.1:c.858G>A, NM_001351397.2:c.858G>A, NM_001351397.1:c.858G>A, NM_001351403.2:c.858G>A, NM_001351403.1:c.858G>A, NM_001387494.1:c.858G>A, NM_001387490.1:c.858G>A, NM_001387492.1:c.858G>A, NM_001387501.1:c.858G>A, NM_001387498.1:c.858G>A, NM_001387512.1:c.858G>A, NM_001387513.1:c.858G>A, NM_001387505.1:c.858G>A, NM_001387489.1:c.858G>A, NM_001387508.1:c.858G>A, NM_001387495.1:c.858G>A, NM_001387509.1:c.858G>A, NM_001387517.1:c.804G>A, NM_001387496.1:c.858G>A, NM_001387484.1:c.858G>A, NM_001387491.1:c.858G>A, NM_001387507.1:c.858G>A, NM_001387506.1:c.858G>A, NM_001387473.1:c.858G>A, XM_047422903.1:c.858G>A, NM_001387511.1:c.858G>A, NM_001387487.1:c.858G>A, NM_001387479.1:c.858G>A, NM_001387483.1:c.858G>A, NM_001387474.1:c.858G>A, NM_001387502.1:c.858G>A, NM_001387510.1:c.858G>A, NM_001387504.1:c.858G>A, NM_001387478.1:c.858G>A, NM_001387488.1:c.858G>A, NM_001387493.1:c.858G>A, NM_001387476.1:c.858G>A, NM_001387477.1:c.858G>A, NM_001387503.1:c.858G>A, NM_001387497.1:c.858G>A, NM_001387516.1:c.804G>A, NM_001387480.1:c.858G>A, NM_001387470.1:c.858G>A, NM_001387472.1:c.858G>A, NM_001387475.1:c.858G>A, NM_001387486.1:c.858G>A, NM_001387482.1:c.858G>A, NM_001387481.1:c.858G>A, NM_001387515.1:c.858G>A, NM_001387518.1:c.804G>A, NM_001387471.1:c.858G>A, NM_001387485.1:c.858G>A, NM_001387514.1:c.858G>A

                              15.

                              rs1450333382 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                9:110875475 (GRCh38)
                                9:113637755 (GRCh37)
                                Canonical SPDI:
                                NC_000009.12:110875474:G:A
                                Gene:
                                LPAR1 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0./0 (ALFA)
                                A=0.000004/1 (TOPMED)
                                A=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000009.12:g.110875475G>A, NC_000009.11:g.113637755G>A, NM_001401.5:c.1041C>T, NM_001401.4:c.1041C>T, NM_001401.3:c.1041C>T, NM_057159.4:c.1041C>T, NM_057159.3:c.1041C>T, NM_057159.2:c.1041C>T, NM_001351410.2:c.1041C>T, NM_001351410.1:c.1041C>T, NM_001351409.2:c.1041C>T, NM_001351409.1:c.1041C>T, NM_001351407.2:c.1041C>T, NM_001351407.1:c.1041C>T, NM_001351413.2:c.1041C>T, NM_001351413.1:c.1041C>T, NM_001351412.2:c.1041C>T, NM_001351412.1:c.1041C>T, NM_001351408.2:c.1041C>T, NM_001351408.1:c.1041C>T, NM_001351415.2:c.1041C>T, NM_001351415.1:c.1041C>T, NM_001351418.2:c.1041C>T, NM_001351418.1:c.1041C>T, NM_001351414.2:c.1041C>T, NM_001351414.1:c.1041C>T, NM_001351416.2:c.1041C>T, NM_001351416.1:c.1041C>T, NM_001351411.2:c.1041C>T, NM_001351411.1:c.1041C>T, NM_001351417.2:c.1041C>T, NM_001351417.1:c.1041C>T, NM_001351398.2:c.1041C>T, NM_001351398.1:c.1041C>T, NM_001351401.2:c.1041C>T, NM_001351401.1:c.1041C>T, NM_001351406.2:c.1041C>T, NM_001351406.1:c.1041C>T, NM_001351400.2:c.1041C>T, NM_001351400.1:c.1041C>T, NM_001351420.2:c.1041C>T, NM_001351420.1:c.1041C>T, NM_001351399.2:c.1041C>T, NM_001351399.1:c.1041C>T, NM_001351402.2:c.1041C>T, NM_001351402.1:c.1041C>T, NM_001351419.2:c.1041C>T, NM_001351419.1:c.1041C>T, NM_001351405.2:c.1041C>T, NM_001351405.1:c.1041C>T, NM_001351404.2:c.1041C>T, NM_001351404.1:c.1041C>T, NM_001351397.2:c.1041C>T, NM_001351397.1:c.1041C>T, NM_001351403.2:c.1041C>T, NM_001351403.1:c.1041C>T, NM_001387494.1:c.1041C>T, NM_001387490.1:c.1041C>T, NM_001387492.1:c.1041C>T, NM_001387501.1:c.1041C>T, NM_001387498.1:c.1041C>T, NM_001387512.1:c.1041C>T, NM_001387513.1:c.1041C>T, NM_001387505.1:c.1041C>T, NM_001387489.1:c.1041C>T, NM_001387508.1:c.1041C>T, NM_001387495.1:c.1041C>T, NM_001387509.1:c.1041C>T, NM_001387517.1:c.987C>T, NM_001387496.1:c.1041C>T, NM_001387484.1:c.1041C>T, NM_001387491.1:c.1041C>T, NM_001387507.1:c.1041C>T, NM_001387506.1:c.1041C>T, NM_001387473.1:c.1041C>T, XM_047422903.1:c.1041C>T, NM_001387511.1:c.1041C>T, NM_001387487.1:c.1041C>T, NM_001387479.1:c.1041C>T, NM_001387483.1:c.1041C>T, NM_001387474.1:c.1041C>T, NM_001387502.1:c.1041C>T, NM_001387510.1:c.1041C>T, NM_001387504.1:c.1041C>T, NM_001387478.1:c.1041C>T, NM_001387488.1:c.1041C>T, NM_001387493.1:c.1041C>T, NM_001387476.1:c.1041C>T, NM_001387477.1:c.1041C>T, NM_001387503.1:c.1041C>T, NM_001387497.1:c.1041C>T, NM_001387516.1:c.987C>T, NM_001387480.1:c.1041C>T, NM_001387470.1:c.1041C>T, NM_001387472.1:c.1041C>T, NM_001387475.1:c.1041C>T, NM_001387486.1:c.1041C>T, NM_001387482.1:c.1041C>T, NM_001387481.1:c.1041C>T, NM_001387515.1:c.1041C>T, NM_001387518.1:c.987C>T, NM_001387471.1:c.1041C>T, NM_001387485.1:c.1041C>T, NM_001387514.1:c.1041C>T

                                16.

                                rs1448755930 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A [Show Flanks]
                                  Chromosome:
                                  9:110941572 (GRCh38)
                                  9:113703852 (GRCh37)
                                  Canonical SPDI:
                                  NC_000009.12:110941571:G:A
                                  Gene:
                                  LPAR1 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,synonymous_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  A=0./0 (ALFA)
                                  A=0.000004/1 (TOPMED)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000009.12:g.110941572G>A, NC_000009.11:g.113703852G>A, NM_001401.5:c.642C>T, NM_001401.4:c.642C>T, NM_001401.3:c.642C>T, NM_057159.4:c.642C>T, NM_057159.3:c.642C>T, NM_057159.2:c.642C>T, NM_001351410.2:c.642C>T, NM_001351410.1:c.642C>T, NM_001351409.2:c.642C>T, NM_001351409.1:c.642C>T, NM_001351407.2:c.642C>T, NM_001351407.1:c.642C>T, NM_001351413.2:c.642C>T, NM_001351413.1:c.642C>T, NM_001351412.2:c.642C>T, NM_001351412.1:c.642C>T, NM_001351408.2:c.642C>T, NM_001351408.1:c.642C>T, NM_001351415.2:c.642C>T, NM_001351415.1:c.642C>T, NM_001351418.2:c.642C>T, NM_001351418.1:c.642C>T, NM_001351414.2:c.642C>T, NM_001351414.1:c.642C>T, NM_001351416.2:c.642C>T, NM_001351416.1:c.642C>T, NM_001351411.2:c.642C>T, NM_001351411.1:c.642C>T, NM_001351417.2:c.642C>T, NM_001351417.1:c.642C>T, NM_001351398.2:c.642C>T, NM_001351398.1:c.642C>T, NM_001351401.2:c.642C>T, NM_001351401.1:c.642C>T, NM_001351406.2:c.642C>T, NM_001351406.1:c.642C>T, NM_001351400.2:c.642C>T, NM_001351400.1:c.642C>T, NM_001351420.2:c.642C>T, NM_001351420.1:c.642C>T, NM_001351399.2:c.642C>T, NM_001351399.1:c.642C>T, NM_001351402.2:c.642C>T, NM_001351402.1:c.642C>T, NM_001351419.2:c.642C>T, NM_001351419.1:c.642C>T, NM_001351405.2:c.642C>T, NM_001351405.1:c.642C>T, NM_001351404.2:c.642C>T, NM_001351404.1:c.642C>T, NM_001351397.2:c.642C>T, NM_001351397.1:c.642C>T, NM_001351403.2:c.642C>T, NM_001351403.1:c.642C>T, NM_001387494.1:c.642C>T, NM_001387490.1:c.642C>T, NM_001387492.1:c.642C>T, NM_001387501.1:c.642C>T, NM_001387498.1:c.642C>T, NM_001387512.1:c.642C>T, NM_001387513.1:c.642C>T, NM_001387505.1:c.642C>T, NM_001387489.1:c.642C>T, NM_001387508.1:c.642C>T, NM_001387495.1:c.642C>T, NM_001387509.1:c.642C>T, NM_001387517.1:c.588C>T, NM_001387496.1:c.642C>T, NM_001387484.1:c.642C>T, NM_001387491.1:c.642C>T, NM_001387507.1:c.642C>T, NM_001387506.1:c.642C>T, NM_001387473.1:c.642C>T, XM_047422903.1:c.642C>T, NM_001387511.1:c.642C>T, NM_001387487.1:c.642C>T, NM_001387479.1:c.642C>T, NM_001387483.1:c.642C>T, NM_001387474.1:c.642C>T, NM_001387502.1:c.642C>T, NM_001387510.1:c.642C>T, NM_001387504.1:c.642C>T, NM_001387478.1:c.642C>T, NM_001387488.1:c.642C>T, NM_001387493.1:c.642C>T, NM_001387476.1:c.642C>T, NM_001387477.1:c.642C>T, NM_001387503.1:c.642C>T, NM_001387497.1:c.642C>T, NM_001387516.1:c.588C>T, NM_001387480.1:c.642C>T, NM_001387470.1:c.642C>T, NM_001387472.1:c.642C>T, NM_001387475.1:c.642C>T, NM_001387486.1:c.642C>T, NM_001387482.1:c.642C>T, NM_001387481.1:c.642C>T, NM_001387515.1:c.642C>T, NM_001387518.1:c.588C>T, NM_001387471.1:c.642C>T, NM_001387485.1:c.642C>T, NM_001387514.1:c.642C>T, NM_001387521.1:c.642C>T, NM_001387520.1:c.642C>T, NM_001387519.1:c.642C>T

                                  17.

                                  rs1447016712 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A,T [Show Flanks]
                                    Chromosome:
                                    9:110941678 (GRCh38)
                                    9:113703958 (GRCh37)
                                    Canonical SPDI:
                                    NC_000009.12:110941677:C:A,NC_000009.12:110941677:C:T
                                    Gene:
                                    LPAR1 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    HGVS:
                                    NC_000009.12:g.110941678C>A, NC_000009.12:g.110941678C>T, NC_000009.11:g.113703958C>A, NC_000009.11:g.113703958C>T, NM_001401.5:c.536G>T, NM_001401.5:c.536G>A, NM_001401.4:c.536G>T, NM_001401.4:c.536G>A, NM_001401.3:c.536G>T, NM_001401.3:c.536G>A, NM_057159.4:c.536G>T, NM_057159.4:c.536G>A, NM_057159.3:c.536G>T, NM_057159.3:c.536G>A, NM_057159.2:c.536G>T, NM_057159.2:c.536G>A, NM_001351410.2:c.536G>T, NM_001351410.2:c.536G>A, NM_001351410.1:c.536G>T, NM_001351410.1:c.536G>A, NM_001351409.2:c.536G>T, NM_001351409.2:c.536G>A, NM_001351409.1:c.536G>T, NM_001351409.1:c.536G>A, NM_001351407.2:c.536G>T, NM_001351407.2:c.536G>A, NM_001351407.1:c.536G>T, NM_001351407.1:c.536G>A, NM_001351413.2:c.536G>T, NM_001351413.2:c.536G>A, NM_001351413.1:c.536G>T, NM_001351413.1:c.536G>A, NM_001351412.2:c.536G>T, NM_001351412.2:c.536G>A, NM_001351412.1:c.536G>T, NM_001351412.1:c.536G>A, NM_001351408.2:c.536G>T, NM_001351408.2:c.536G>A, NM_001351408.1:c.536G>T, NM_001351408.1:c.536G>A, NM_001351415.2:c.536G>T, NM_001351415.2:c.536G>A, NM_001351415.1:c.536G>T, NM_001351415.1:c.536G>A, NM_001351418.2:c.536G>T, NM_001351418.2:c.536G>A, NM_001351418.1:c.536G>T, NM_001351418.1:c.536G>A, NM_001351414.2:c.536G>T, NM_001351414.2:c.536G>A, NM_001351414.1:c.536G>T, NM_001351414.1:c.536G>A, NM_001351416.2:c.536G>T, NM_001351416.2:c.536G>A, NM_001351416.1:c.536G>T, NM_001351416.1:c.536G>A, NM_001351411.2:c.536G>T, NM_001351411.2:c.536G>A, NM_001351411.1:c.536G>T, NM_001351411.1:c.536G>A, NM_001351417.2:c.536G>T, NM_001351417.2:c.536G>A, NM_001351417.1:c.536G>T, NM_001351417.1:c.536G>A, NM_001351398.2:c.536G>T, NM_001351398.2:c.536G>A, NM_001351398.1:c.536G>T, NM_001351398.1:c.536G>A, NM_001351401.2:c.536G>T, NM_001351401.2:c.536G>A, NM_001351401.1:c.536G>T, NM_001351401.1:c.536G>A, NM_001351406.2:c.536G>T, NM_001351406.2:c.536G>A, NM_001351406.1:c.536G>T, NM_001351406.1:c.536G>A, NM_001351400.2:c.536G>T, NM_001351400.2:c.536G>A, NM_001351400.1:c.536G>T, NM_001351400.1:c.536G>A, NM_001351420.2:c.536G>T, NM_001351420.2:c.536G>A, NM_001351420.1:c.536G>T, NM_001351420.1:c.536G>A, NM_001351399.2:c.536G>T, NM_001351399.2:c.536G>A, NM_001351399.1:c.536G>T, NM_001351399.1:c.536G>A, NM_001351402.2:c.536G>T, NM_001351402.2:c.536G>A, NM_001351402.1:c.536G>T, NM_001351402.1:c.536G>A, NM_001351419.2:c.536G>T, NM_001351419.2:c.536G>A, NM_001351419.1:c.536G>T, NM_001351419.1:c.536G>A, NM_001351405.2:c.536G>T, NM_001351405.2:c.536G>A, NM_001351405.1:c.536G>T, NM_001351405.1:c.536G>A, NM_001351404.2:c.536G>T, NM_001351404.2:c.536G>A, NM_001351404.1:c.536G>T, NM_001351404.1:c.536G>A, NM_001351397.2:c.536G>T, NM_001351397.2:c.536G>A, NM_001351397.1:c.536G>T, NM_001351397.1:c.536G>A, NM_001351403.2:c.536G>T, NM_001351403.2:c.536G>A, NM_001351403.1:c.536G>T, NM_001351403.1:c.536G>A, NM_001387494.1:c.536G>T, NM_001387494.1:c.536G>A, NM_001387490.1:c.536G>T, NM_001387490.1:c.536G>A, NM_001387492.1:c.536G>T, NM_001387492.1:c.536G>A, NM_001387501.1:c.536G>T, NM_001387501.1:c.536G>A, NM_001387498.1:c.536G>T, NM_001387498.1:c.536G>A, NM_001387512.1:c.536G>T, NM_001387512.1:c.536G>A, NM_001387513.1:c.536G>T, NM_001387513.1:c.536G>A, NM_001387505.1:c.536G>T, NM_001387505.1:c.536G>A, NM_001387489.1:c.536G>T, NM_001387489.1:c.536G>A, NM_001387508.1:c.536G>T, NM_001387508.1:c.536G>A, NM_001387495.1:c.536G>T, NM_001387495.1:c.536G>A, NM_001387509.1:c.536G>T, NM_001387509.1:c.536G>A, NM_001387517.1:c.482G>T, NM_001387517.1:c.482G>A, NM_001387496.1:c.536G>T, NM_001387496.1:c.536G>A, NM_001387484.1:c.536G>T, NM_001387484.1:c.536G>A, NM_001387491.1:c.536G>T, NM_001387491.1:c.536G>A, NM_001387507.1:c.536G>T, NM_001387507.1:c.536G>A, NM_001387506.1:c.536G>T, NM_001387506.1:c.536G>A, NM_001387473.1:c.536G>T, NM_001387473.1:c.536G>A, XM_047422903.1:c.536G>T, XM_047422903.1:c.536G>A, NM_001387511.1:c.536G>T, NM_001387511.1:c.536G>A, NM_001387487.1:c.536G>T, NM_001387487.1:c.536G>A, NM_001387479.1:c.536G>T, NM_001387479.1:c.536G>A, NM_001387483.1:c.536G>T, NM_001387483.1:c.536G>A, NM_001387474.1:c.536G>T, NM_001387474.1:c.536G>A, NM_001387502.1:c.536G>T, NM_001387502.1:c.536G>A, NM_001387510.1:c.536G>T, NM_001387510.1:c.536G>A, NM_001387504.1:c.536G>T, NM_001387504.1:c.536G>A, NM_001387478.1:c.536G>T, NM_001387478.1:c.536G>A, NM_001387488.1:c.536G>T, NM_001387488.1:c.536G>A, NM_001387493.1:c.536G>T, NM_001387493.1:c.536G>A, NM_001387476.1:c.536G>T, NM_001387476.1:c.536G>A, NM_001387477.1:c.536G>T, NM_001387477.1:c.536G>A, NM_001387503.1:c.536G>T, NM_001387503.1:c.536G>A, NM_001387497.1:c.536G>T, NM_001387497.1:c.536G>A, NM_001387516.1:c.482G>T, NM_001387516.1:c.482G>A, NM_001387480.1:c.536G>T, NM_001387480.1:c.536G>A, NM_001387470.1:c.536G>T, NM_001387470.1:c.536G>A, NM_001387472.1:c.536G>T, NM_001387472.1:c.536G>A, NM_001387475.1:c.536G>T, NM_001387475.1:c.536G>A, NM_001387486.1:c.536G>T, NM_001387486.1:c.536G>A, NM_001387482.1:c.536G>T, NM_001387482.1:c.536G>A, NM_001387481.1:c.536G>T, NM_001387481.1:c.536G>A, NM_001387515.1:c.536G>T, NM_001387515.1:c.536G>A, NM_001387518.1:c.482G>T, NM_001387518.1:c.482G>A, NM_001387471.1:c.536G>T, NM_001387471.1:c.536G>A, NM_001387485.1:c.536G>T, NM_001387485.1:c.536G>A, NM_001387514.1:c.536G>T, NM_001387514.1:c.536G>A, NM_001387521.1:c.536G>T, NM_001387521.1:c.536G>A, NM_001387520.1:c.536G>T, NM_001387520.1:c.536G>A, NM_001387519.1:c.536G>T, NM_001387519.1:c.536G>A, NP_001392.2:p.Gly179Val, NP_001392.2:p.Gly179Asp, NP_476500.1:p.Gly179Val, NP_476500.1:p.Gly179Asp, NP_001338339.1:p.Gly179Val, NP_001338339.1:p.Gly179Asp, NP_001338338.1:p.Gly179Val, NP_001338338.1:p.Gly179Asp, NP_001338336.1:p.Gly179Val, NP_001338336.1:p.Gly179Asp, NP_001338342.1:p.Gly179Val, NP_001338342.1:p.Gly179Asp, NP_001338341.1:p.Gly179Val, NP_001338341.1:p.Gly179Asp, NP_001338337.1:p.Gly179Val, NP_001338337.1:p.Gly179Asp, NP_001338344.1:p.Gly179Val, NP_001338344.1:p.Gly179Asp, NP_001338347.1:p.Gly179Val, NP_001338347.1:p.Gly179Asp, NP_001338343.1:p.Gly179Val, NP_001338343.1:p.Gly179Asp, NP_001338345.1:p.Gly179Val, NP_001338345.1:p.Gly179Asp, NP_001338340.1:p.Gly179Val, NP_001338340.1:p.Gly179Asp, NP_001338346.1:p.Gly179Val, NP_001338346.1:p.Gly179Asp, NP_001338327.1:p.Gly179Val, NP_001338327.1:p.Gly179Asp, NP_001338330.1:p.Gly179Val, NP_001338330.1:p.Gly179Asp, NP_001338335.1:p.Gly179Val, NP_001338335.1:p.Gly179Asp, NP_001338329.1:p.Gly179Val, NP_001338329.1:p.Gly179Asp, NP_001338349.1:p.Gly179Val, NP_001338349.1:p.Gly179Asp, NP_001338328.1:p.Gly179Val, NP_001338328.1:p.Gly179Asp, NP_001338331.1:p.Gly179Val, NP_001338331.1:p.Gly179Asp, NP_001338348.1:p.Gly179Val, NP_001338348.1:p.Gly179Asp, NP_001338334.1:p.Gly179Val, NP_001338334.1:p.Gly179Asp, NP_001338333.1:p.Gly179Val, NP_001338333.1:p.Gly179Asp, NP_001338326.1:p.Gly179Val, NP_001338326.1:p.Gly179Asp, NP_001338332.1:p.Gly179Val, NP_001338332.1:p.Gly179Asp, NP_001374423.1:p.Gly179Val, NP_001374423.1:p.Gly179Asp, NP_001374419.1:p.Gly179Val, NP_001374419.1:p.Gly179Asp, NP_001374421.1:p.Gly179Val, NP_001374421.1:p.Gly179Asp, NP_001374430.1:p.Gly179Val, NP_001374430.1:p.Gly179Asp, NP_001374427.1:p.Gly179Val, NP_001374427.1:p.Gly179Asp, NP_001374441.1:p.Gly179Val, NP_001374441.1:p.Gly179Asp, NP_001374442.1:p.Gly179Val, NP_001374442.1:p.Gly179Asp, NP_001374434.1:p.Gly179Val, NP_001374434.1:p.Gly179Asp, NP_001374418.1:p.Gly179Val, NP_001374418.1:p.Gly179Asp, NP_001374437.1:p.Gly179Val, NP_001374437.1:p.Gly179Asp, NP_001374424.1:p.Gly179Val, NP_001374424.1:p.Gly179Asp, NP_001374438.1:p.Gly179Val, NP_001374438.1:p.Gly179Asp, NP_001374446.1:p.Gly161Val, NP_001374446.1:p.Gly161Asp, NP_001374425.1:p.Gly179Val, NP_001374425.1:p.Gly179Asp, NP_001374413.1:p.Gly179Val, NP_001374413.1:p.Gly179Asp, NP_001374420.1:p.Gly179Val, NP_001374420.1:p.Gly179Asp, NP_001374436.1:p.Gly179Val, NP_001374436.1:p.Gly179Asp, NP_001374435.1:p.Gly179Val, NP_001374435.1:p.Gly179Asp, NP_001374402.1:p.Gly179Val, NP_001374402.1:p.Gly179Asp, XP_047278859.1:p.Gly179Val, XP_047278859.1:p.Gly179Asp, NP_001374440.1:p.Gly179Val, NP_001374440.1:p.Gly179Asp, NP_001374416.1:p.Gly179Val, NP_001374416.1:p.Gly179Asp, NP_001374408.1:p.Gly179Val, NP_001374408.1:p.Gly179Asp, NP_001374412.1:p.Gly179Val, NP_001374412.1:p.Gly179Asp, NP_001374403.1:p.Gly179Val, NP_001374403.1:p.Gly179Asp, NP_001374431.1:p.Gly179Val, NP_001374431.1:p.Gly179Asp, NP_001374439.1:p.Gly179Val, NP_001374439.1:p.Gly179Asp, NP_001374433.1:p.Gly179Val, NP_001374433.1:p.Gly179Asp, NP_001374407.1:p.Gly179Val, NP_001374407.1:p.Gly179Asp, NP_001374417.1:p.Gly179Val, NP_001374417.1:p.Gly179Asp, NP_001374422.1:p.Gly179Val, NP_001374422.1:p.Gly179Asp, NP_001374405.1:p.Gly179Val, NP_001374405.1:p.Gly179Asp, NP_001374406.1:p.Gly179Val, NP_001374406.1:p.Gly179Asp, NP_001374432.1:p.Gly179Val, NP_001374432.1:p.Gly179Asp, NP_001374426.1:p.Gly179Val, NP_001374426.1:p.Gly179Asp, NP_001374445.1:p.Gly161Val, NP_001374445.1:p.Gly161Asp, NP_001374409.1:p.Gly179Val, NP_001374409.1:p.Gly179Asp, NP_001374399.1:p.Gly179Val, NP_001374399.1:p.Gly179Asp, NP_001374401.1:p.Gly179Val, NP_001374401.1:p.Gly179Asp, NP_001374404.1:p.Gly179Val, NP_001374404.1:p.Gly179Asp, NP_001374415.1:p.Gly179Val, NP_001374415.1:p.Gly179Asp, NP_001374411.1:p.Gly179Val, NP_001374411.1:p.Gly179Asp, NP_001374410.1:p.Gly179Val, NP_001374410.1:p.Gly179Asp, NP_001374444.1:p.Gly179Val, NP_001374444.1:p.Gly179Asp, NP_001374447.1:p.Gly161Val, NP_001374447.1:p.Gly161Asp, NP_001374400.1:p.Gly179Val, NP_001374400.1:p.Gly179Asp, NP_001374414.1:p.Gly179Val, NP_001374414.1:p.Gly179Asp, NP_001374443.1:p.Gly179Val, NP_001374443.1:p.Gly179Asp, NP_001374450.1:p.Gly179Val, NP_001374450.1:p.Gly179Asp, NP_001374449.1:p.Gly179Val, NP_001374449.1:p.Gly179Asp, NP_001374448.1:p.Gly179Val, NP_001374448.1:p.Gly179Asp

                                    18.

                                    rs1443986033 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      9:110942114 (GRCh38)
                                      9:113704394 (GRCh37)
                                      Canonical SPDI:
                                      NC_000009.12:110942113:A:G
                                      Gene:
                                      LPAR1 (Varview)
                                      Functional Consequence:
                                      missense_variant,coding_sequence_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      G=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000009.12:g.110942114A>G, NC_000009.11:g.113704394A>G, NM_001401.5:c.100T>C, NM_001401.4:c.100T>C, NM_001401.3:c.100T>C, NM_057159.4:c.100T>C, NM_057159.3:c.100T>C, NM_057159.2:c.100T>C, NM_001351410.2:c.100T>C, NM_001351410.1:c.100T>C, NM_001351409.2:c.100T>C, NM_001351409.1:c.100T>C, NM_001351407.2:c.100T>C, NM_001351407.1:c.100T>C, NM_001351413.2:c.100T>C, NM_001351413.1:c.100T>C, NM_001351412.2:c.100T>C, NM_001351412.1:c.100T>C, NM_001351408.2:c.100T>C, NM_001351408.1:c.100T>C, NM_001351415.2:c.100T>C, NM_001351415.1:c.100T>C, NM_001351418.2:c.100T>C, NM_001351418.1:c.100T>C, NM_001351414.2:c.100T>C, NM_001351414.1:c.100T>C, NM_001351416.2:c.100T>C, NM_001351416.1:c.100T>C, NM_001351411.2:c.100T>C, NM_001351411.1:c.100T>C, NM_001351417.2:c.100T>C, NM_001351417.1:c.100T>C, NM_001351398.2:c.100T>C, NM_001351398.1:c.100T>C, NM_001351401.2:c.100T>C, NM_001351401.1:c.100T>C, NM_001351406.2:c.100T>C, NM_001351406.1:c.100T>C, NM_001351400.2:c.100T>C, NM_001351400.1:c.100T>C, NM_001351420.2:c.100T>C, NM_001351420.1:c.100T>C, NM_001351399.2:c.100T>C, NM_001351399.1:c.100T>C, NM_001351402.2:c.100T>C, NM_001351402.1:c.100T>C, NM_001351419.2:c.100T>C, NM_001351419.1:c.100T>C, NM_001351405.2:c.100T>C, NM_001351405.1:c.100T>C, NM_001351404.2:c.100T>C, NM_001351404.1:c.100T>C, NM_001351397.2:c.100T>C, NM_001351397.1:c.100T>C, NM_001351403.2:c.100T>C, NM_001351403.1:c.100T>C, NM_001387494.1:c.100T>C, NM_001387490.1:c.100T>C, NM_001387492.1:c.100T>C, NM_001387501.1:c.100T>C, NM_001387498.1:c.100T>C, NM_001387512.1:c.100T>C, NM_001387513.1:c.100T>C, NM_001387505.1:c.100T>C, NM_001387489.1:c.100T>C, NM_001387508.1:c.100T>C, NM_001387495.1:c.100T>C, NM_001387509.1:c.100T>C, NM_001387517.1:c.46T>C, NM_001387496.1:c.100T>C, NM_001387484.1:c.100T>C, NM_001387491.1:c.100T>C, NM_001387507.1:c.100T>C, NM_001387506.1:c.100T>C, NM_001387473.1:c.100T>C, XM_047422903.1:c.100T>C, NM_001387511.1:c.100T>C, NM_001387487.1:c.100T>C, NM_001387479.1:c.100T>C, NM_001387483.1:c.100T>C, NM_001387474.1:c.100T>C, NM_001387502.1:c.100T>C, NM_001387510.1:c.100T>C, NM_001387504.1:c.100T>C, NM_001387478.1:c.100T>C, NM_001387488.1:c.100T>C, NM_001387493.1:c.100T>C, NM_001387476.1:c.100T>C, NM_001387477.1:c.100T>C, NM_001387503.1:c.100T>C, NM_001387497.1:c.100T>C, NM_001387516.1:c.46T>C, NM_001387480.1:c.100T>C, NM_001387470.1:c.100T>C, NM_001387472.1:c.100T>C, NM_001387475.1:c.100T>C, NM_001387486.1:c.100T>C, NM_001387482.1:c.100T>C, NM_001387481.1:c.100T>C, NM_001387515.1:c.100T>C, NM_001387518.1:c.46T>C, NM_001387471.1:c.100T>C, NM_001387485.1:c.100T>C, NM_001387514.1:c.100T>C, NM_001387521.1:c.100T>C, NM_001387520.1:c.100T>C, NM_001387519.1:c.100T>C, NP_001392.2:p.Tyr34His, NP_476500.1:p.Tyr34His, NP_001338339.1:p.Tyr34His, NP_001338338.1:p.Tyr34His, NP_001338336.1:p.Tyr34His, NP_001338342.1:p.Tyr34His, NP_001338341.1:p.Tyr34His, NP_001338337.1:p.Tyr34His, NP_001338344.1:p.Tyr34His, NP_001338347.1:p.Tyr34His, NP_001338343.1:p.Tyr34His, NP_001338345.1:p.Tyr34His, NP_001338340.1:p.Tyr34His, NP_001338346.1:p.Tyr34His, NP_001338327.1:p.Tyr34His, NP_001338330.1:p.Tyr34His, NP_001338335.1:p.Tyr34His, NP_001338329.1:p.Tyr34His, NP_001338349.1:p.Tyr34His, NP_001338328.1:p.Tyr34His, NP_001338331.1:p.Tyr34His, NP_001338348.1:p.Tyr34His, NP_001338334.1:p.Tyr34His, NP_001338333.1:p.Tyr34His, NP_001338326.1:p.Tyr34His, NP_001338332.1:p.Tyr34His, NP_001374423.1:p.Tyr34His, NP_001374419.1:p.Tyr34His, NP_001374421.1:p.Tyr34His, NP_001374430.1:p.Tyr34His, NP_001374427.1:p.Tyr34His, NP_001374441.1:p.Tyr34His, NP_001374442.1:p.Tyr34His, NP_001374434.1:p.Tyr34His, NP_001374418.1:p.Tyr34His, NP_001374437.1:p.Tyr34His, NP_001374424.1:p.Tyr34His, NP_001374438.1:p.Tyr34His, NP_001374446.1:p.Tyr16His, NP_001374425.1:p.Tyr34His, NP_001374413.1:p.Tyr34His, NP_001374420.1:p.Tyr34His, NP_001374436.1:p.Tyr34His, NP_001374435.1:p.Tyr34His, NP_001374402.1:p.Tyr34His, XP_047278859.1:p.Tyr34His, NP_001374440.1:p.Tyr34His, NP_001374416.1:p.Tyr34His, NP_001374408.1:p.Tyr34His, NP_001374412.1:p.Tyr34His, NP_001374403.1:p.Tyr34His, NP_001374431.1:p.Tyr34His, NP_001374439.1:p.Tyr34His, NP_001374433.1:p.Tyr34His, NP_001374407.1:p.Tyr34His, NP_001374417.1:p.Tyr34His, NP_001374422.1:p.Tyr34His, NP_001374405.1:p.Tyr34His, NP_001374406.1:p.Tyr34His, NP_001374432.1:p.Tyr34His, NP_001374426.1:p.Tyr34His, NP_001374445.1:p.Tyr16His, NP_001374409.1:p.Tyr34His, NP_001374399.1:p.Tyr34His, NP_001374401.1:p.Tyr34His, NP_001374404.1:p.Tyr34His, NP_001374415.1:p.Tyr34His, NP_001374411.1:p.Tyr34His, NP_001374410.1:p.Tyr34His, NP_001374444.1:p.Tyr34His, NP_001374447.1:p.Tyr16His, NP_001374400.1:p.Tyr34His, NP_001374414.1:p.Tyr34His, NP_001374443.1:p.Tyr34His, NP_001374450.1:p.Tyr34His, NP_001374449.1:p.Tyr34His, NP_001374448.1:p.Tyr34His

                                      19.

                                      rs1439964419 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>A [Show Flanks]
                                        Chromosome:
                                        9:110875592 (GRCh38)
                                        9:113637872 (GRCh37)
                                        Canonical SPDI:
                                        NC_000009.12:110875591:G:A
                                        Gene:
                                        LPAR1 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        A=0.000007/1 (GnomAD)
                                        HGVS:
                                        NC_000009.12:g.110875592G>A, NC_000009.11:g.113637872G>A, NM_001401.5:c.924C>T, NM_001401.4:c.924C>T, NM_001401.3:c.924C>T, NM_057159.4:c.924C>T, NM_057159.3:c.924C>T, NM_057159.2:c.924C>T, NM_001351410.2:c.924C>T, NM_001351410.1:c.924C>T, NM_001351409.2:c.924C>T, NM_001351409.1:c.924C>T, NM_001351407.2:c.924C>T, NM_001351407.1:c.924C>T, NM_001351413.2:c.924C>T, NM_001351413.1:c.924C>T, NM_001351412.2:c.924C>T, NM_001351412.1:c.924C>T, NM_001351408.2:c.924C>T, NM_001351408.1:c.924C>T, NM_001351415.2:c.924C>T, NM_001351415.1:c.924C>T, NM_001351418.2:c.924C>T, NM_001351418.1:c.924C>T, NM_001351414.2:c.924C>T, NM_001351414.1:c.924C>T, NM_001351416.2:c.924C>T, NM_001351416.1:c.924C>T, NM_001351411.2:c.924C>T, NM_001351411.1:c.924C>T, NM_001351417.2:c.924C>T, NM_001351417.1:c.924C>T, NM_001351398.2:c.924C>T, NM_001351398.1:c.924C>T, NM_001351401.2:c.924C>T, NM_001351401.1:c.924C>T, NM_001351406.2:c.924C>T, NM_001351406.1:c.924C>T, NM_001351400.2:c.924C>T, NM_001351400.1:c.924C>T, NM_001351420.2:c.924C>T, NM_001351420.1:c.924C>T, NM_001351399.2:c.924C>T, NM_001351399.1:c.924C>T, NM_001351402.2:c.924C>T, NM_001351402.1:c.924C>T, NM_001351419.2:c.924C>T, NM_001351419.1:c.924C>T, NM_001351405.2:c.924C>T, NM_001351405.1:c.924C>T, NM_001351404.2:c.924C>T, NM_001351404.1:c.924C>T, NM_001351397.2:c.924C>T, NM_001351397.1:c.924C>T, NM_001351403.2:c.924C>T, NM_001351403.1:c.924C>T, NM_001387494.1:c.924C>T, NM_001387490.1:c.924C>T, NM_001387492.1:c.924C>T, NM_001387501.1:c.924C>T, NM_001387498.1:c.924C>T, NM_001387512.1:c.924C>T, NM_001387513.1:c.924C>T, NM_001387505.1:c.924C>T, NM_001387489.1:c.924C>T, NM_001387508.1:c.924C>T, NM_001387495.1:c.924C>T, NM_001387509.1:c.924C>T, NM_001387517.1:c.870C>T, NM_001387496.1:c.924C>T, NM_001387484.1:c.924C>T, NM_001387491.1:c.924C>T, NM_001387507.1:c.924C>T, NM_001387506.1:c.924C>T, NM_001387473.1:c.924C>T, XM_047422903.1:c.924C>T, NM_001387511.1:c.924C>T, NM_001387487.1:c.924C>T, NM_001387479.1:c.924C>T, NM_001387483.1:c.924C>T, NM_001387474.1:c.924C>T, NM_001387502.1:c.924C>T, NM_001387510.1:c.924C>T, NM_001387504.1:c.924C>T, NM_001387478.1:c.924C>T, NM_001387488.1:c.924C>T, NM_001387493.1:c.924C>T, NM_001387476.1:c.924C>T, NM_001387477.1:c.924C>T, NM_001387503.1:c.924C>T, NM_001387497.1:c.924C>T, NM_001387516.1:c.870C>T, NM_001387480.1:c.924C>T, NM_001387470.1:c.924C>T, NM_001387472.1:c.924C>T, NM_001387475.1:c.924C>T, NM_001387486.1:c.924C>T, NM_001387482.1:c.924C>T, NM_001387481.1:c.924C>T, NM_001387515.1:c.924C>T, NM_001387518.1:c.870C>T, NM_001387471.1:c.924C>T, NM_001387485.1:c.924C>T, NM_001387514.1:c.924C>T

                                        20.

                                        rs1427698580 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          9:110942016 (GRCh38)
                                          9:113704296 (GRCh37)
                                          Canonical SPDI:
                                          NC_000009.12:110942015:G:A
                                          Gene:
                                          LPAR1 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant
                                          Validated:
                                          by frequency,by cluster
                                          MAF:
                                          A=0.000008/2 (GnomAD_exomes)
                                          A=0.000546/1 (Korea1K)
                                          HGVS:
                                          NC_000009.12:g.110942016G>A, NC_000009.11:g.113704296G>A, NM_001401.5:c.198C>T, NM_001401.4:c.198C>T, NM_001401.3:c.198C>T, NM_057159.4:c.198C>T, NM_057159.3:c.198C>T, NM_057159.2:c.198C>T, NM_001351410.2:c.198C>T, NM_001351410.1:c.198C>T, NM_001351409.2:c.198C>T, NM_001351409.1:c.198C>T, NM_001351407.2:c.198C>T, NM_001351407.1:c.198C>T, NM_001351413.2:c.198C>T, NM_001351413.1:c.198C>T, NM_001351412.2:c.198C>T, NM_001351412.1:c.198C>T, NM_001351408.2:c.198C>T, NM_001351408.1:c.198C>T, NM_001351415.2:c.198C>T, NM_001351415.1:c.198C>T, NM_001351418.2:c.198C>T, NM_001351418.1:c.198C>T, NM_001351414.2:c.198C>T, NM_001351414.1:c.198C>T, NM_001351416.2:c.198C>T, NM_001351416.1:c.198C>T, NM_001351411.2:c.198C>T, NM_001351411.1:c.198C>T, NM_001351417.2:c.198C>T, NM_001351417.1:c.198C>T, NM_001351398.2:c.198C>T, NM_001351398.1:c.198C>T, NM_001351401.2:c.198C>T, NM_001351401.1:c.198C>T, NM_001351406.2:c.198C>T, NM_001351406.1:c.198C>T, NM_001351400.2:c.198C>T, NM_001351400.1:c.198C>T, NM_001351420.2:c.198C>T, NM_001351420.1:c.198C>T, NM_001351399.2:c.198C>T, NM_001351399.1:c.198C>T, NM_001351402.2:c.198C>T, NM_001351402.1:c.198C>T, NM_001351419.2:c.198C>T, NM_001351419.1:c.198C>T, NM_001351405.2:c.198C>T, NM_001351405.1:c.198C>T, NM_001351404.2:c.198C>T, NM_001351404.1:c.198C>T, NM_001351397.2:c.198C>T, NM_001351397.1:c.198C>T, NM_001351403.2:c.198C>T, NM_001351403.1:c.198C>T, NM_001387494.1:c.198C>T, NM_001387490.1:c.198C>T, NM_001387492.1:c.198C>T, NM_001387501.1:c.198C>T, NM_001387498.1:c.198C>T, NM_001387512.1:c.198C>T, NM_001387513.1:c.198C>T, NM_001387505.1:c.198C>T, NM_001387489.1:c.198C>T, NM_001387508.1:c.198C>T, NM_001387495.1:c.198C>T, NM_001387509.1:c.198C>T, NM_001387517.1:c.144C>T, NM_001387496.1:c.198C>T, NM_001387484.1:c.198C>T, NM_001387491.1:c.198C>T, NM_001387507.1:c.198C>T, NM_001387506.1:c.198C>T, NM_001387473.1:c.198C>T, XM_047422903.1:c.198C>T, NM_001387511.1:c.198C>T, NM_001387487.1:c.198C>T, NM_001387479.1:c.198C>T, NM_001387483.1:c.198C>T, NM_001387474.1:c.198C>T, NM_001387502.1:c.198C>T, NM_001387510.1:c.198C>T, NM_001387504.1:c.198C>T, NM_001387478.1:c.198C>T, NM_001387488.1:c.198C>T, NM_001387493.1:c.198C>T, NM_001387476.1:c.198C>T, NM_001387477.1:c.198C>T, NM_001387503.1:c.198C>T, NM_001387497.1:c.198C>T, NM_001387516.1:c.144C>T, NM_001387480.1:c.198C>T, NM_001387470.1:c.198C>T, NM_001387472.1:c.198C>T, NM_001387475.1:c.198C>T, NM_001387486.1:c.198C>T, NM_001387482.1:c.198C>T, NM_001387481.1:c.198C>T, NM_001387515.1:c.198C>T, NM_001387518.1:c.144C>T, NM_001387471.1:c.198C>T, NM_001387485.1:c.198C>T, NM_001387514.1:c.198C>T, NM_001387521.1:c.198C>T, NM_001387520.1:c.198C>T, NM_001387519.1:c.198C>T

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