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Items: 1 to 20 of 1000

1.

rs1491350077 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    CT>- [Show Flanks]
    Chromosome:
    19:54224471 (GRCh38)
    19:54728344 (GRCh37)
    Canonical SPDI:
    NC_000019.10:54224470:CT:
    Gene:
    LILRB3 (Varview), LOC124904768 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0./0 (ALFA)
    -=0.000007/1 (GnomAD)
    -=0.000312/2 (1000Genomes)
    HGVS:

    2.

    rs1491292372 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->TG [Show Flanks]
      Chromosome:
      19:54224471 (GRCh38)
      19:54728344 (GRCh37)
      Canonical SPDI:
      NC_000019.10:54224471:TGTGTGTGTG:TGTGTGTGTGTG
      Gene:
      LILRB3 (Varview), LOC124904768 (Varview)
      Functional Consequence:
      2KB_upstream_variant,upstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      TGTGTGTGTGTG=0./0 (ALFA)
      HGVS:

      3.

      rs1491186177 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        TG>- [Show Flanks]
        Chromosome:
        19:54219987 (GRCh38)
        19:54723856 (GRCh37)
        Canonical SPDI:
        NC_000019.10:54219986:TG:
        Gene:
        LILRB3 (Varview), LOC124904768 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by cluster
        MAF:
        -=0.0022/18 (ExAC)
        HGVS:

        4.

        rs1490910902 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>C,T [Show Flanks]
          Chromosome:
          19:54220570 (GRCh38)
          19:54724440 (GRCh37)
          Canonical SPDI:
          NC_000019.10:54220569:G:C,NC_000019.10:54220569:G:T
          Gene:
          LILRB3 (Varview), LOC124904768 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.00001/1 (GnomAD)
          C=0.000312/2 (1000Genomes)
          HGVS:
          NC_000019.10:g.54220570G>C, NC_000019.10:g.54220570G>T, NW_004166865.1:g.194937G>C, NW_004166865.1:g.194937G>T, NW_003571061.2:g.195554G>C, NW_003571061.2:g.195554G>T, NW_003571055.2:g.195554G>C, NW_003571055.2:g.195554G>T, NW_003571061.1:g.195553G>C, NW_003571061.1:g.195553G>T, NW_003571059.2:g.195554G>C, NW_003571059.2:g.195554G>T, NW_003571056.2:g.195554G>C, NW_003571056.2:g.195554G>T, NW_003571057.2:g.195554G>C, NW_003571057.2:g.195554G>T, NW_003571058.2:g.195554G>C, NW_003571058.2:g.195554G>T, NT_187693.1:g.195554G>C, NT_187693.1:g.195554G>T, NC_000019.9:g.54724440G>C, NC_000019.9:g.54724440G>T, NW_003571060.1:g.195558G>C, NW_003571060.1:g.195558G>T, NW_003571054.1:g.195370G>C, NW_003571054.1:g.195370G>T, XM_006726314.5:c.1216C>G, XM_006726314.5:c.1216C>A, XM_006726314.4:c.1216C>G, XM_006726314.4:c.1216C>A, XM_006726314.3:c.1216C>G, XM_006726314.3:c.1216C>A, XM_006726314.2:c.1216C>G, XM_006726314.2:c.1216C>A, XM_006726314.1:c.1216C>G, XM_006726314.1:c.1216C>A, XM_006726313.5:c.1216C>G, XM_006726313.5:c.1216C>A, XM_006726313.4:c.1216C>G, XM_006726313.4:c.1216C>A, XM_006726313.3:c.1216C>G, XM_006726313.3:c.1216C>A, XM_006726313.2:c.1216C>G, XM_006726313.2:c.1216C>A, XM_006726313.1:c.1216C>G, XM_006726313.1:c.1216C>A, XM_011548574.4:c.1216C>G, XM_011548574.4:c.1216C>A, XM_011548574.3:c.1216C>G, XM_011548574.3:c.1216C>A, XM_011548574.2:c.1216C>G, XM_011548574.2:c.1216C>A, XM_011548574.1:c.1216C>G, XM_011548574.1:c.1216C>A, NM_006864.4:c.1216C>G, NM_006864.4:c.1216C>A, NM_006864.3:c.1216C>G, NM_006864.3:c.1216C>A, not_yet_implemented, not_yet_implemented, not_yet_implemented, XM_011548575.4:c.1216C>G, XM_011548575.4:c.1216C>A, XM_011548575.3:c.1216C>G, XM_011548575.3:c.1216C>A, XM_011548575.2:c.1216C>G, XM_011548575.2:c.1216C>A, XM_011548575.1:c.1216C>G, XM_011548575.1:c.1216C>A, XM_011547051.4:c.1216C>G, XM_011547051.4:c.1216C>A, XM_011547051.3:c.1216C>G, XM_011547051.3:c.1216C>A, XM_011547051.2:c.1216C>G, XM_011547051.2:c.1216C>A, XM_011547051.1:c.1216C>G, XM_011547051.1:c.1216C>A, XR_952182.4:n.1297C>G, XR_952182.4:n.1297C>A, XR_952182.3:n.1296C>G, XR_952182.3:n.1296C>A, XR_952182.2:n.1296C>G, XR_952182.2:n.1296C>A, XR_952182.1:n.1273C>G, XR_952182.1:n.1273C>A, XM_011526382.3:c.1216C>G, XM_011526382.3:c.1216C>A, XM_011526382.2:c.1216C>G, XM_011526382.2:c.1216C>A, XM_011526382.1:c.1216C>G, XM_011526382.1:c.1216C>A, XM_011526381.3:c.1216C>G, XM_011526381.3:c.1216C>A, XM_011526381.2:c.1216C>G, XM_011526381.2:c.1216C>A, XM_011526381.1:c.1216C>G, XM_011526381.1:c.1216C>A, NM_001081450.3:c.1216C>G, NM_001081450.3:c.1216C>A, NM_001081450.2:c.1216C>G, NM_001081450.2:c.1216C>A, not_yet_implemented, not_yet_implemented, not_yet_implemented, XM_011547058.3:c.1216C>G, XM_011547058.3:c.1216C>A, XM_011547058.2:c.1216C>G, XM_011547058.2:c.1216C>A, XM_011547058.1:c.1216C>G, XM_011547058.1:c.1216C>A, XM_006726278.3:c.1216C>G, XM_006726278.3:c.1216C>A, XM_006726278.2:c.1216C>G, XM_006726278.2:c.1216C>A, XM_006726278.1:c.1216C>G, XM_006726278.1:c.1216C>A, XM_006726280.3:c.1216C>G, XM_006726280.3:c.1216C>A, XM_006726280.2:c.1216C>G, XM_006726280.2:c.1216C>A, XM_006726280.1:c.1216C>G, XM_006726280.1:c.1216C>A, NR_135496.2:n.1330C>G, NR_135496.2:n.1330C>A, NR_135496.1:n.1410C>G, NR_135496.1:n.1410C>A, NM_001320960.2:c.1216C>G, NM_001320960.2:c.1216C>A, NM_001320960.1:c.1216C>G, NM_001320960.1:c.1216C>A, NR_135493.2:n.1247C>G, NR_135493.2:n.1247C>A, NR_135493.1:n.1327C>G, NR_135493.1:n.1327C>A, NR_135495.2:n.1167C>G, NR_135495.2:n.1167C>A, NR_135495.1:n.1247C>G, NR_135495.1:n.1247C>A, NR_135494.2:n.1161C>G, NR_135494.2:n.1161C>A, NR_135494.1:n.1241C>G, NR_135494.1:n.1241C>A, XM_047438108.1:c.1216C>G, XM_047438108.1:c.1216C>A, XM_047438111.1:c.1216C>G, XM_047438111.1:c.1216C>A, XM_017030296.2:c.1216C>G, XM_017030296.2:c.1216C>A, XM_017030296.1:c.1216C>G, XM_017030296.1:c.1216C>A, XM_017030297.2:c.1216C>G, XM_017030297.2:c.1216C>A, XM_017030297.1:c.1216C>G, XM_017030297.1:c.1216C>A, XR_001756804.2:n.1349C>G, XR_001756804.2:n.1349C>A, XR_001756804.1:n.1327C>G, XR_001756804.1:n.1327C>A, XM_047438110.1:c.1216C>G, XM_047438110.1:c.1216C>A, XM_047443025.1:c.70C>G, XM_047443025.1:c.70C>A, XM_047442999.1:c.70C>G, XM_047442999.1:c.70C>A, XM_047442982.1:c.70C>G, XM_047442982.1:c.70C>A, XM_011547050.3:c.1216C>G, XM_011547050.3:c.1216C>A, XM_011547050.2:c.1216C>G, XM_011547050.2:c.1216C>A, XM_011547050.1:c.1216C>G, XM_011547050.1:c.1216C>A, XM_047438109.1:c.1216C>G, XM_047438109.1:c.1216C>A, XM_047442986.1:c.70C>G, XM_047442986.1:c.70C>A, XM_047443035.1:c.1216C>G, XM_047443035.1:c.1216C>A, XM_047443420.1:c.1216C>G, XM_047443420.1:c.1216C>A, XM_047443421.1:c.1216C>G, XM_047443421.1:c.1216C>A, XM_047443036.1:c.1216C>G, XM_047443036.1:c.1216C>A, XM_047442913.1:c.1216C>G, XM_047442913.1:c.1216C>A, XR_007068731.1:n.1297C>G, XR_007068731.1:n.1297C>A, XR_007068898.1:n.1335C>G, XR_007068898.1:n.1335C>A, NP_006855.3:p.Leu406Val, NP_006855.3:p.Leu406Met, XP_011524684.1:p.Leu406Val, XP_011524684.1:p.Leu406Met, XP_011524683.1:p.Leu406Val, XP_011524683.1:p.Leu406Met, NP_001074919.2:p.Leu406Val, NP_001074919.2:p.Leu406Met, NP_001307889.1:p.Leu406Val, NP_001307889.1:p.Leu406Met, XP_047294064.1:p.Leu406Val, XP_047294064.1:p.Leu406Met, XP_047294067.1:p.Leu406Val, XP_047294067.1:p.Leu406Met, XP_047294066.1:p.Leu406Val, XP_047294066.1:p.Leu406Met, XP_047294065.1:p.Leu406Val, XP_047294065.1:p.Leu406Met

          5.

          rs1490168922 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>T [Show Flanks]
            Chromosome:
            19:54222056 (GRCh38)
            19:54725928 (GRCh37)
            Canonical SPDI:
            NC_000019.10:54222055:A:T
            Gene:
            LILRB3 (Varview), LOC124904768 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
            Validated:
            by frequency,by alfa
            MAF:
            T=0./0 (ALFA)
            HGVS:
            NC_000019.10:g.54222056A>T, NW_004166865.1:g.196423A>T, NT_187693.1:g.197042A>T, NC_000019.9:g.54725928A>T, NW_003571060.1:g.197046A>T, NW_003571054.1:g.196856A>T, XM_006726314.5:c.430T>A, XM_006726314.4:c.430T>A, XM_006726314.3:c.430T>A, XM_006726314.2:c.430T>A, XM_006726314.1:c.430T>A, XM_006726313.5:c.430T>A, XM_006726313.4:c.430T>A, XM_006726313.3:c.430T>A, XM_006726313.2:c.430T>A, XM_006726313.1:c.430T>A, NM_006864.4:c.430T>A, NM_006864.3:c.430T>A, not_yet_implemented, not_yet_implemented, XM_011547051.4:c.430T>A, XM_011547051.3:c.430T>A, XM_011547051.2:c.430T>A, XM_011547051.1:c.430T>A, XM_011526382.3:c.430T>A, XM_011526382.2:c.430T>A, XM_011526382.1:c.430T>A, XM_011548574.4:c.430T>A, XM_011548574.3:c.430T>A, XM_011548574.2:c.430T>A, XM_011548574.1:c.430T>A, XM_011548575.4:c.430T>A, XM_011548575.3:c.430T>A, XM_011548575.2:c.430T>A, XM_011548575.1:c.430T>A, XR_952182.4:n.511T>A, XR_952182.3:n.510T>A, XR_952182.2:n.510T>A, XR_952182.1:n.487T>A, XM_011526381.3:c.430T>A, XM_011526381.2:c.430T>A, XM_011526381.1:c.430T>A, NM_001081450.3:c.430T>A, NM_001081450.2:c.430T>A, not_yet_implemented, not_yet_implemented, XM_011547058.3:c.430T>A, XM_011547058.2:c.430T>A, XM_011547058.1:c.430T>A, XM_006726278.3:c.430T>A, XM_006726278.2:c.430T>A, XM_006726278.1:c.430T>A, XM_006726280.3:c.430T>A, XM_006726280.2:c.430T>A, XM_006726280.1:c.430T>A, NR_135495.2:n.461T>A, NR_135495.1:n.541T>A, NR_135494.2:n.461T>A, NR_135494.1:n.541T>A, XM_011547050.3:c.430T>A, XM_011547050.2:c.430T>A, XM_011547050.1:c.430T>A, NR_135493.2:n.461T>A, NR_135493.1:n.541T>A, NR_135496.2:n.461T>A, NR_135496.1:n.541T>A, XM_017030297.2:c.430T>A, XM_017030297.1:c.430T>A, XR_001756804.2:n.563T>A, XR_001756804.1:n.541T>A, XM_047438108.1:c.430T>A, XM_047438109.1:c.430T>A, XM_047438111.1:c.430T>A, NM_001320960.2:c.430T>A, NM_001320960.1:c.430T>A, XM_017030296.2:c.430T>A, XM_017030296.1:c.430T>A, XM_047438110.1:c.430T>A, XM_047443035.1:c.430T>A, XM_047443420.1:c.430T>A, XM_047443421.1:c.430T>A, XM_047443036.1:c.430T>A, XM_047442913.1:c.430T>A, XR_007068731.1:n.511T>A, XR_007068898.1:n.549T>A, NP_006855.3:p.Cys144Ser, XP_011524684.1:p.Cys144Ser, XP_011524683.1:p.Cys144Ser, NP_001074919.2:p.Cys144Ser, XP_047294064.1:p.Cys144Ser, XP_047294065.1:p.Cys144Ser, XP_047294067.1:p.Cys144Ser, NP_001307889.1:p.Cys144Ser, XP_047294066.1:p.Cys144Ser

            6.

            rs1490056594 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              19:54221420 (GRCh38)
              19:54725292 (GRCh37)
              Canonical SPDI:
              NC_000019.10:54221419:T:C
              Gene:
              LILRB3 (Varview), LOC124904768 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              C=0./0 (ALFA)
              C=0.000004/1 (TOPMED)
              HGVS:

              7.

              rs1489938415 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>A,C [Show Flanks]
                Chromosome:
                19:54220572 (GRCh38)
                19:54724442 (GRCh37)
                Canonical SPDI:
                NC_000019.10:54220571:T:A,NC_000019.10:54220571:T:C
                Gene:
                LILRB3 (Varview), LOC124904768 (Varview)
                Functional Consequence:
                non_coding_transcript_variant,missense_variant,intron_variant,coding_sequence_variant
                Validated:
                by frequency,by cluster
                MAF:
                C=0.0002/1 (1000Genomes)
                HGVS:
                NC_000019.10:g.54220572T>A, NC_000019.10:g.54220572T>C, NW_004166865.1:g.194939T>A, NW_004166865.1:g.194939T>C, NW_003571061.2:g.195556T>A, NW_003571061.2:g.195556T>C, NW_003571055.2:g.195556T>A, NW_003571055.2:g.195556T>C, NW_003571061.1:g.195555T>A, NW_003571061.1:g.195555T>C, NW_003571059.2:g.195556T>A, NW_003571059.2:g.195556T>C, NW_003571056.2:g.195556T>A, NW_003571056.2:g.195556T>C, NW_003571057.2:g.195556T>A, NW_003571057.2:g.195556T>C, NW_003571058.2:g.195556T>A, NW_003571058.2:g.195556T>C, NT_187693.1:g.195556T>A, NT_187693.1:g.195556T>C, NC_000019.9:g.54724442T>A, NC_000019.9:g.54724442T>C, NW_003571060.1:g.195560T>A, NW_003571060.1:g.195560T>C, NW_003571054.1:g.195372T>A, NW_003571054.1:g.195372T>C, XM_006726314.5:c.1214A>T, XM_006726314.5:c.1214A>G, XM_006726314.4:c.1214A>T, XM_006726314.4:c.1214A>G, XM_006726314.3:c.1214A>T, XM_006726314.3:c.1214A>G, XM_006726314.2:c.1214A>T, XM_006726314.2:c.1214A>G, XM_006726314.1:c.1214A>T, XM_006726314.1:c.1214A>G, XM_006726313.5:c.1214A>T, XM_006726313.5:c.1214A>G, XM_006726313.4:c.1214A>T, XM_006726313.4:c.1214A>G, XM_006726313.3:c.1214A>T, XM_006726313.3:c.1214A>G, XM_006726313.2:c.1214A>T, XM_006726313.2:c.1214A>G, XM_006726313.1:c.1214A>T, XM_006726313.1:c.1214A>G, XM_011548574.4:c.1214A>T, XM_011548574.4:c.1214A>G, XM_011548574.3:c.1214A>T, XM_011548574.3:c.1214A>G, XM_011548574.2:c.1214A>T, XM_011548574.2:c.1214A>G, XM_011548574.1:c.1214A>T, XM_011548574.1:c.1214A>G, NM_006864.4:c.1214A>T, NM_006864.4:c.1214A>G, NM_006864.3:c.1214A>T, NM_006864.3:c.1214A>G, not_yet_implemented, not_yet_implemented, not_yet_implemented, XM_011548575.4:c.1214A>T, XM_011548575.4:c.1214A>G, XM_011548575.3:c.1214A>T, XM_011548575.3:c.1214A>G, XM_011548575.2:c.1214A>T, XM_011548575.2:c.1214A>G, XM_011548575.1:c.1214A>T, XM_011548575.1:c.1214A>G, XM_011547051.4:c.1214A>T, XM_011547051.4:c.1214A>G, XM_011547051.3:c.1214A>T, XM_011547051.3:c.1214A>G, XM_011547051.2:c.1214A>T, XM_011547051.2:c.1214A>G, XM_011547051.1:c.1214A>T, XM_011547051.1:c.1214A>G, XR_952182.4:n.1295A>T, XR_952182.4:n.1295A>G, XR_952182.3:n.1294A>T, XR_952182.3:n.1294A>G, XR_952182.2:n.1294A>T, XR_952182.2:n.1294A>G, XR_952182.1:n.1271A>T, XR_952182.1:n.1271A>G, XM_011526382.3:c.1214A>T, XM_011526382.3:c.1214A>G, XM_011526382.2:c.1214A>T, XM_011526382.2:c.1214A>G, XM_011526382.1:c.1214A>T, XM_011526382.1:c.1214A>G, XM_011526381.3:c.1214A>T, XM_011526381.3:c.1214A>G, XM_011526381.2:c.1214A>T, XM_011526381.2:c.1214A>G, XM_011526381.1:c.1214A>T, XM_011526381.1:c.1214A>G, NM_001081450.3:c.1214A>T, NM_001081450.3:c.1214A>G, NM_001081450.2:c.1214A>T, NM_001081450.2:c.1214A>G, not_yet_implemented, not_yet_implemented, not_yet_implemented, XM_011547058.3:c.1214A>T, XM_011547058.3:c.1214A>G, XM_011547058.2:c.1214A>T, XM_011547058.2:c.1214A>G, XM_011547058.1:c.1214A>T, XM_011547058.1:c.1214A>G, XM_006726278.3:c.1214A>T, XM_006726278.3:c.1214A>G, XM_006726278.2:c.1214A>T, XM_006726278.2:c.1214A>G, XM_006726278.1:c.1214A>T, XM_006726278.1:c.1214A>G, XM_006726280.3:c.1214A>T, XM_006726280.3:c.1214A>G, XM_006726280.2:c.1214A>T, XM_006726280.2:c.1214A>G, XM_006726280.1:c.1214A>T, XM_006726280.1:c.1214A>G, NR_135496.2:n.1328A>T, NR_135496.2:n.1328A>G, NR_135496.1:n.1408A>T, NR_135496.1:n.1408A>G, NM_001320960.2:c.1214A>T, NM_001320960.2:c.1214A>G, NM_001320960.1:c.1214A>T, NM_001320960.1:c.1214A>G, NR_135493.2:n.1245A>T, NR_135493.2:n.1245A>G, NR_135493.1:n.1325A>T, NR_135493.1:n.1325A>G, NR_135495.2:n.1165A>T, NR_135495.2:n.1165A>G, NR_135495.1:n.1245A>T, NR_135495.1:n.1245A>G, NR_135494.2:n.1159A>T, NR_135494.2:n.1159A>G, NR_135494.1:n.1239A>T, NR_135494.1:n.1239A>G, XM_047438108.1:c.1214A>T, XM_047438108.1:c.1214A>G, XM_047438111.1:c.1214A>T, XM_047438111.1:c.1214A>G, XM_017030296.2:c.1214A>T, XM_017030296.2:c.1214A>G, XM_017030296.1:c.1214A>T, XM_017030296.1:c.1214A>G, XM_017030297.2:c.1214A>T, XM_017030297.2:c.1214A>G, XM_017030297.1:c.1214A>T, XM_017030297.1:c.1214A>G, XR_001756804.2:n.1347A>T, XR_001756804.2:n.1347A>G, XR_001756804.1:n.1325A>T, XR_001756804.1:n.1325A>G, XM_047438110.1:c.1214A>T, XM_047438110.1:c.1214A>G, XM_047443025.1:c.68A>T, XM_047443025.1:c.68A>G, XM_047442999.1:c.68A>T, XM_047442999.1:c.68A>G, XM_047442982.1:c.68A>T, XM_047442982.1:c.68A>G, XM_011547050.3:c.1214A>T, XM_011547050.3:c.1214A>G, XM_011547050.2:c.1214A>T, XM_011547050.2:c.1214A>G, XM_011547050.1:c.1214A>T, XM_011547050.1:c.1214A>G, XM_047438109.1:c.1214A>T, XM_047438109.1:c.1214A>G, XM_047442986.1:c.68A>T, XM_047442986.1:c.68A>G, XM_047443035.1:c.1214A>T, XM_047443035.1:c.1214A>G, XM_047443420.1:c.1214A>T, XM_047443420.1:c.1214A>G, XM_047443421.1:c.1214A>T, XM_047443421.1:c.1214A>G, XM_047443036.1:c.1214A>T, XM_047443036.1:c.1214A>G, XM_047442913.1:c.1214A>T, XM_047442913.1:c.1214A>G, XR_007068731.1:n.1295A>T, XR_007068731.1:n.1295A>G, XR_007068898.1:n.1333A>T, XR_007068898.1:n.1333A>G, NP_006855.3:p.His405Leu, NP_006855.3:p.His405Arg, XP_011524684.1:p.His405Leu, XP_011524684.1:p.His405Arg, XP_011524683.1:p.His405Leu, XP_011524683.1:p.His405Arg, NP_001074919.2:p.His405Leu, NP_001074919.2:p.His405Arg, NP_001307889.1:p.His405Leu, NP_001307889.1:p.His405Arg, XP_047294064.1:p.His405Leu, XP_047294064.1:p.His405Arg, XP_047294067.1:p.His405Leu, XP_047294067.1:p.His405Arg, XP_047294066.1:p.His405Leu, XP_047294066.1:p.His405Arg, XP_047294065.1:p.His405Leu, XP_047294065.1:p.His405Arg

                8.

                rs1489879889 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>T [Show Flanks]
                  Chromosome:
                  19:54221652 (GRCh38)
                  19:54725524 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:54221651:C:T
                  Gene:
                  LILRB3 (Varview), LOC124904768 (Varview)
                  Functional Consequence:
                  non_coding_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0.000084/1 (ALFA)
                  T=0.000022/3 (GnomAD)
                  T=0.000023/6 (TOPMED)
                  T=0.000106/2 (TOMMO)
                  T=0.001032/3 (KOREAN)
                  HGVS:

                  9.

                  rs1489804402 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    19:54222938 (GRCh38)
                    19:54726810 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:54222937:C:T
                    Gene:
                    LILRB3 (Varview), LOC124904768 (Varview)
                    Functional Consequence:
                    intron_variant
                    HGVS:

                    10.

                    rs1488825576 [Homo sapiens]
                      Variant type:
                      SNV:
                      Alleles:
                      A>-
                      Chromosome:
                      no mapping
                      Canonical SPDI:

                      11.

                      rs1488270732 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        19:54224374 (GRCh38)
                        19:54728246 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:54224373:C:T
                        Gene:
                        LILRB3 (Varview), LOC124904768 (Varview)
                        Functional Consequence:
                        2KB_upstream_variant,upstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000044/6 (GnomAD)
                        HGVS:

                        12.

                        rs1488174151 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          19:54215818 (GRCh38)
                          19:54719687 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:54215817:C:T
                          Gene:
                          LILRB3 (Varview)
                          Functional Consequence:
                          downstream_transcript_variant,500B_downstream_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000004/1 (TOPMED)
                          HGVS:

                          13.

                          rs1488092944 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>G,T [Show Flanks]
                            Chromosome:
                            19:54222744 (GRCh38)
                            19:54726616 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:54222743:C:G,NC_000019.10:54222743:C:T
                            Gene:
                            LILRB3 (Varview), LOC124904768 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000014/2 (GnomAD)
                            G=0.000019/5 (TOPMED)
                            T=0.000625/4 (1000Genomes)
                            T=0.001947/55 (TOMMO)
                            HGVS:

                            14.

                            rs1487970433 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>A,G [Show Flanks]
                              Chromosome:
                              19:54220878 (GRCh38)
                              19:54724748 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:54220877:C:A,NC_000019.10:54220877:C:G
                              Gene:
                              LILRB3 (Varview), LOC124904768 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0.000084/1 (ALFA)
                              G=0.000019/5 (TOPMED)
                              C=0.5/1 (SGDP_PRJ)
                              HGVS:

                              15.

                              rs1487961532 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>G,T [Show Flanks]
                                Chromosome:
                                19:54218614 (GRCh38)
                                19:54722483 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:54218613:C:G,NC_000019.10:54218613:C:T
                                Gene:
                                LILRB3 (Varview), LOC124904768 (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,genic_downstream_transcript_variant,downstream_transcript_variant,missense_variant,coding_sequence_variant,upstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.000071/1 (ALFA)
                                T=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000019.10:g.54218614C>G, NC_000019.10:g.54218614C>T, NW_004166865.1:g.192981C>G, NW_004166865.1:g.192981C>T, NW_003571061.2:g.193597C>G, NW_003571061.2:g.193597C>T, NW_003571055.2:g.193597C>G, NW_003571055.2:g.193597C>T, NW_003571061.1:g.193596C>G, NW_003571061.1:g.193596C>T, NW_003571059.2:g.193597C>G, NW_003571059.2:g.193597C>T, NW_003571056.2:g.193597C>G, NW_003571056.2:g.193597C>T, NW_003571057.2:g.193597C>G, NW_003571057.2:g.193597C>T, NW_003571058.2:g.193597C>G, NW_003571058.2:g.193597C>T, NT_187693.1:g.193597C>G, NT_187693.1:g.193597C>T, NC_000019.9:g.54722483C>G, NC_000019.9:g.54722483C>T, NW_003571060.1:g.193600C>G, NW_003571060.1:g.193600C>T, NW_003571054.1:g.193414C>G, NW_003571054.1:g.193414C>T, XM_047442999.1:c.425G>C, XM_047442999.1:c.425G>A, XM_047438108.1:c.1571G>C, XM_047438108.1:c.1571G>A, XM_047443415.1:c.416G>C, XM_047443415.1:c.416G>A, XM_047442965.1:c.416G>C, XM_047442965.1:c.416G>A, XM_047443025.1:c.425G>C, XM_047443025.1:c.425G>A, XM_047442966.1:c.416G>C, XM_047442966.1:c.416G>A, XM_047442986.1:c.425G>C, XM_047442986.1:c.425G>A, XM_047442982.1:c.425G>C, XM_047442982.1:c.425G>A, XM_047443035.1:c.1571G>C, XM_047443035.1:c.1571G>A, XM_047443420.1:c.1571G>C, XM_047443420.1:c.1571G>A, XM_047443421.1:c.1571G>C, XM_047443421.1:c.1571G>A, XM_047443036.1:c.1571G>C, XM_047443036.1:c.1571G>A, XP_047294064.1:p.Cys524Ser, XP_047294064.1:p.Cys524Tyr

                                16.

                                rs1487846313 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>G [Show Flanks]
                                  Chromosome:
                                  19:54223800 (GRCh38)
                                  19:54727672 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:54223799:A:G
                                  Gene:
                                  LILRB3 (Varview), LOC124904768 (Varview)
                                  Functional Consequence:
                                  2KB_upstream_variant,upstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  G=0.000071/1 (ALFA)
                                  G=0.000007/1 (GnomAD)
                                  G=0.000008/2 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1487816770 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>G [Show Flanks]
                                    Chromosome:
                                    19:54223608 (GRCh38)
                                    19:54727480 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:54223607:T:G
                                    Gene:
                                    LILRB3 (Varview), LOC124904768 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0.005985/71 (ALFA)
                                    G=0.002967/19 (1000Genomes)
                                    G=0.004149/577 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1487584320 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      19:54215833 (GRCh38)
                                      19:54719702 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:54215832:C:T
                                      Gene:
                                      LILRB3 (Varview)
                                      Functional Consequence:
                                      downstream_transcript_variant,500B_downstream_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000007/1 (GnomAD)
                                      T=0.000015/4 (TOPMED)
                                      T=0.000035/1 (TOMMO)
                                      HGVS:

                                      19.

                                      rs1487327109 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        19:54217903 (GRCh38)
                                        19:54721772 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:54217902:A:G
                                        Gene:
                                        LILRB3 (Varview), LOC124904768 (Varview)
                                        Functional Consequence:
                                        2KB_upstream_variant,genic_downstream_transcript_variant,upstream_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        G=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1487057265 [Homo sapiens]
                                          Variant type:
                                          INS
                                          Alleles:
                                          ->AG,G,TG [Show Flanks]
                                          Chromosome:
                                          19:54220949 (GRCh38)
                                          19:-1 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:54220949::AG,NC_000019.10:54220949::G,NC_000019.10:54220949::TG
                                          Gene:
                                          LILRB3 (Varview), LOC124904768 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TG=0.00034/4 (ALFA)
                                          HGVS:

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