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1.

rs1491568648 has merged into rs35016569 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TGTGTGTGTGTG>-,TG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
    Chromosome:
    8:11422359 (GRCh38)
    8:11279868 (GRCh37)
    Canonical SPDI:
    NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:11422355:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG
    Gene:
    FAM167A (Varview), FAM167A-AS1 (Varview)
    Functional Consequence:
    intron_variant,3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    GTGTG=0./0 (ALFA)
    -=0.000004/1 (TOPMED)
    GT=0.000035/1 (TOMMO)
    -=0.075/3 (GENOME_DK)
    HGVS:
    NC_000008.11:g.11422357TG[1], NC_000008.11:g.11422357TG[2], NC_000008.11:g.11422357TG[5], NC_000008.11:g.11422357TG[6], NC_000008.11:g.11422357TG[8], NC_000008.11:g.11422357TG[9], NC_000008.11:g.11422357TG[10], NC_000008.11:g.11422357TG[11], NC_000008.11:g.11422357TG[12], NC_000008.10:g.11279866TG[1], NC_000008.10:g.11279866TG[2], NC_000008.10:g.11279866TG[5], NC_000008.10:g.11279866TG[6], NC_000008.10:g.11279866TG[8], NC_000008.10:g.11279866TG[9], NC_000008.10:g.11279866TG[10], NC_000008.10:g.11279866TG[11], NC_000008.10:g.11279866TG[12], NW_018654717.1:g.1926205AC[1], NW_018654717.1:g.1926205AC[2], NW_018654717.1:g.1926205AC[5], NW_018654717.1:g.1926205AC[6], NW_018654717.1:g.1926205AC[8], NW_018654717.1:g.1926205AC[9], NW_018654717.1:g.1926205AC[10], NW_018654717.1:g.1926205AC[11], NW_018654717.1:g.1926205AC[12], XM_005272398.6:c.*2004AC[1], XM_005272398.6:c.*2004AC[2], XM_005272398.6:c.*2004AC[5], XM_005272398.6:c.*2004AC[6], XM_005272398.6:c.*2004AC[8], XM_005272398.6:c.*2004AC[9], XM_005272398.6:c.*2004AC[10], XM_005272398.6:c.*2004AC[11], XM_005272398.6:c.*2004AC[12], XM_005272398.5:c.*2004AC[1], XM_005272398.5:c.*2004AC[2], XM_005272398.5:c.*2004AC[5], XM_005272398.5:c.*2004AC[6], XM_005272398.5:c.*2004AC[8], XM_005272398.5:c.*2004AC[9], XM_005272398.5:c.*2004AC[10], XM_005272398.5:c.*2004AC[11], XM_005272398.5:c.*2004AC[12], XM_005272398.4:c.*2004AC[1], XM_005272398.4:c.*2004AC[2], XM_005272398.4:c.*2004AC[5], XM_005272398.4:c.*2004AC[6], XM_005272398.4:c.*2004AC[8], XM_005272398.4:c.*2004AC[9], XM_005272398.4:c.*2004AC[10], XM_005272398.4:c.*2004AC[11], XM_005272398.4:c.*2004AC[12], XM_005272398.3:c.*2004AC[1], XM_005272398.3:c.*2004AC[2], XM_005272398.3:c.*2004AC[5], XM_005272398.3:c.*2004AC[6], XM_005272398.3:c.*2004AC[8], XM_005272398.3:c.*2004AC[9], XM_005272398.3:c.*2004AC[10], XM_005272398.3:c.*2004AC[11], XM_005272398.3:c.*2004AC[12], XM_005272398.2:c.*2004AC[1], XM_005272398.2:c.*2004AC[2], XM_005272398.2:c.*2004AC[5], XM_005272398.2:c.*2004AC[6], XM_005272398.2:c.*2004AC[8], XM_005272398.2:c.*2004AC[9], XM_005272398.2:c.*2004AC[10], XM_005272398.2:c.*2004AC[11], XM_005272398.2:c.*2004AC[12], XM_005272398.1:c.*2004AC[1], XM_005272398.1:c.*2004AC[2], XM_005272398.1:c.*2004AC[5], XM_005272398.1:c.*2004AC[6], XM_005272398.1:c.*2004AC[8], XM_005272398.1:c.*2004AC[9], XM_005272398.1:c.*2004AC[10], XM_005272398.1:c.*2004AC[11], XM_005272398.1:c.*2004AC[12], XM_011543840.4:c.*2004AC[1], XM_011543840.4:c.*2004AC[2], XM_011543840.4:c.*2004AC[5], XM_011543840.4:c.*2004AC[6], XM_011543840.4:c.*2004AC[8], XM_011543840.4:c.*2004AC[9], XM_011543840.4:c.*2004AC[10], XM_011543840.4:c.*2004AC[11], XM_011543840.4:c.*2004AC[12], XM_011543840.3:c.*2004AC[1], XM_011543840.3:c.*2004AC[2], XM_011543840.3:c.*2004AC[5], XM_011543840.3:c.*2004AC[6], XM_011543840.3:c.*2004AC[8], XM_011543840.3:c.*2004AC[9], XM_011543840.3:c.*2004AC[10], XM_011543840.3:c.*2004AC[11], XM_011543840.3:c.*2004AC[12], XM_011543840.2:c.*2004AC[1], XM_011543840.2:c.*2004AC[2], XM_011543840.2:c.*2004AC[5], XM_011543840.2:c.*2004AC[6], XM_011543840.2:c.*2004AC[8], XM_011543840.2:c.*2004AC[9], XM_011543840.2:c.*2004AC[10], XM_011543840.2:c.*2004AC[11], XM_011543840.2:c.*2004AC[12], XM_011543840.1:c.*2004AC[1], XM_011543840.1:c.*2004AC[2], XM_011543840.1:c.*2004AC[5], XM_011543840.1:c.*2004AC[6], XM_011543840.1:c.*2004AC[8], XM_011543840.1:c.*2004AC[9], XM_011543840.1:c.*2004AC[10], XM_011543840.1:c.*2004AC[11], XM_011543840.1:c.*2004AC[12], XM_011543838.4:c.*2004AC[1], XM_011543838.4:c.*2004AC[2], XM_011543838.4:c.*2004AC[5], XM_011543838.4:c.*2004AC[6], XM_011543838.4:c.*2004AC[8], XM_011543838.4:c.*2004AC[9], XM_011543838.4:c.*2004AC[10], XM_011543838.4:c.*2004AC[11], XM_011543838.4:c.*2004AC[12], XM_011543838.3:c.*2004AC[1], XM_011543838.3:c.*2004AC[2], XM_011543838.3:c.*2004AC[5], XM_011543838.3:c.*2004AC[6], XM_011543838.3:c.*2004AC[8], XM_011543838.3:c.*2004AC[9], XM_011543838.3:c.*2004AC[10], XM_011543838.3:c.*2004AC[11], XM_011543838.3:c.*2004AC[12], XM_011543838.2:c.*2004AC[1], XM_011543838.2:c.*2004AC[2], XM_011543838.2:c.*2004AC[5], XM_011543838.2:c.*2004AC[6], XM_011543838.2:c.*2004AC[8], XM_011543838.2:c.*2004AC[9], XM_011543838.2:c.*2004AC[10], XM_011543838.2:c.*2004AC[11], XM_011543838.2:c.*2004AC[12], XM_011543838.1:c.*2004AC[1], XM_011543838.1:c.*2004AC[2], XM_011543838.1:c.*2004AC[5], XM_011543838.1:c.*2004AC[6], XM_011543838.1:c.*2004AC[8], XM_011543838.1:c.*2004AC[9], XM_011543838.1:c.*2004AC[10], XM_011543838.1:c.*2004AC[11], XM_011543838.1:c.*2004AC[12], NM_053279.3:c.*2004AC[1], NM_053279.3:c.*2004AC[2], NM_053279.3:c.*2004AC[5], NM_053279.3:c.*2004AC[6], NM_053279.3:c.*2004AC[8], NM_053279.3:c.*2004AC[9], NM_053279.3:c.*2004AC[10], NM_053279.3:c.*2004AC[11], NM_053279.3:c.*2004AC[12], NM_053279.2:c.*2004AC[1], NM_053279.2:c.*2004AC[2], NM_053279.2:c.*2004AC[5], NM_053279.2:c.*2004AC[6], NM_053279.2:c.*2004AC[8], NM_053279.2:c.*2004AC[9], NM_053279.2:c.*2004AC[10], NM_053279.2:c.*2004AC[11], NM_053279.2:c.*2004AC[12], XM_011543837.2:c.*2004AC[1], XM_011543837.2:c.*2004AC[2], XM_011543837.2:c.*2004AC[5], XM_011543837.2:c.*2004AC[6], XM_011543837.2:c.*2004AC[8], XM_011543837.2:c.*2004AC[9], XM_011543837.2:c.*2004AC[10], XM_011543837.2:c.*2004AC[11], XM_011543837.2:c.*2004AC[12], XM_011543837.1:c.*2004AC[1], XM_011543837.1:c.*2004AC[2], XM_011543837.1:c.*2004AC[5], XM_011543837.1:c.*2004AC[6], XM_011543837.1:c.*2004AC[8], XM_011543837.1:c.*2004AC[9], XM_011543837.1:c.*2004AC[10], XM_011543837.1:c.*2004AC[11], XM_011543837.1:c.*2004AC[12], XM_024447292.2:c.*2004AC[1], XM_024447292.2:c.*2004AC[2], XM_024447292.2:c.*2004AC[5], XM_024447292.2:c.*2004AC[6], XM_024447292.2:c.*2004AC[8], XM_024447292.2:c.*2004AC[9], XM_024447292.2:c.*2004AC[10], XM_024447292.2:c.*2004AC[11], XM_024447292.2:c.*2004AC[12], XM_024447292.1:c.*2004AC[1], XM_024447292.1:c.*2004AC[2], XM_024447292.1:c.*2004AC[5], XM_024447292.1:c.*2004AC[6], XM_024447292.1:c.*2004AC[8], XM_024447292.1:c.*2004AC[9], XM_024447292.1:c.*2004AC[10], XM_024447292.1:c.*2004AC[11], XM_024447292.1:c.*2004AC[12]

    2.

    rs1491508132 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      CT>- [Show Flanks]
      Chromosome:
      8:11427653 (GRCh38)
      8:11285162 (GRCh37)
      Canonical SPDI:
      NC_000008.11:11427651:TCT:T
      Gene:
      FAM167A (Varview), FAM167A-AS1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      T=0./0 (ALFA)
      -=0.000007/1 (GnomAD)
      HGVS:

      3.

      rs1491432187 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->T,TGT,TGTGT,TGTGTGTGTGT [Show Flanks]
        Chromosome:
        8:11422370 (GRCh38)
        8:11279880 (GRCh37)
        Canonical SPDI:
        NC_000008.11:11422370::T,NC_000008.11:11422370::TGT,NC_000008.11:11422370::TGTGT,NC_000008.11:11422370::TGTGTGTGTGT
        Gene:
        FAM167A (Varview), FAM167A-AS1 (Varview)
        Functional Consequence:
        intron_variant,3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        TGT=0./0 (ALFA)
        TGT=0.000004/1 (TOPMED)
        T=0.212838/126 (NorthernSweden)
        HGVS:
        NC_000008.11:g.11422370_11422371insT, NC_000008.11:g.11422370_11422371insTGT, NC_000008.11:g.11422370_11422371insTGTGT, NC_000008.11:g.11422370_11422371insTGTGTGTGTGT, NC_000008.10:g.11279879_11279880insT, NC_000008.10:g.11279879_11279880insTGT, NC_000008.10:g.11279879_11279880insTGTGT, NC_000008.10:g.11279879_11279880insTGTGTGTGTGT, NW_018654717.1:g.1926203_1926204insA, NW_018654717.1:g.1926203_1926204insACA, NW_018654717.1:g.1926203_1926204insACACA, NW_018654717.1:g.1926203_1926204insACACACACACA, XM_005272398.6:c.*2002_*2003insA, XM_005272398.6:c.*2002_*2003insACA, XM_005272398.6:c.*2002_*2003insACACA, XM_005272398.6:c.*2002_*2003insACACACACACA, XM_005272398.5:c.*2002_*2003insA, XM_005272398.5:c.*2002_*2003insACA, XM_005272398.5:c.*2002_*2003insACACA, XM_005272398.5:c.*2002_*2003insACACACACACA, XM_005272398.4:c.*2002_*2003insA, XM_005272398.4:c.*2002_*2003insACA, XM_005272398.4:c.*2002_*2003insACACA, XM_005272398.4:c.*2002_*2003insACACACACACA, XM_005272398.3:c.*2002_*2003insA, XM_005272398.3:c.*2002_*2003insACA, XM_005272398.3:c.*2002_*2003insACACA, XM_005272398.3:c.*2002_*2003insACACACACACA, XM_005272398.2:c.*2002_*2003insA, XM_005272398.2:c.*2002_*2003insACA, XM_005272398.2:c.*2002_*2003insACACA, XM_005272398.2:c.*2002_*2003insACACACACACA, XM_005272398.1:c.*2002_*2003insA, XM_005272398.1:c.*2002_*2003insACA, XM_005272398.1:c.*2002_*2003insACACA, XM_005272398.1:c.*2002_*2003insACACACACACA, XM_011543840.4:c.*2002_*2003insA, XM_011543840.4:c.*2002_*2003insACA, XM_011543840.4:c.*2002_*2003insACACA, XM_011543840.4:c.*2002_*2003insACACACACACA, XM_011543840.3:c.*2002_*2003insA, XM_011543840.3:c.*2002_*2003insACA, XM_011543840.3:c.*2002_*2003insACACA, XM_011543840.3:c.*2002_*2003insACACACACACA, XM_011543840.2:c.*2002_*2003insA, XM_011543840.2:c.*2002_*2003insACA, XM_011543840.2:c.*2002_*2003insACACA, XM_011543840.2:c.*2002_*2003insACACACACACA, XM_011543840.1:c.*2002_*2003insA, XM_011543840.1:c.*2002_*2003insACA, XM_011543840.1:c.*2002_*2003insACACA, XM_011543840.1:c.*2002_*2003insACACACACACA, XM_011543838.4:c.*2002_*2003insA, XM_011543838.4:c.*2002_*2003insACA, XM_011543838.4:c.*2002_*2003insACACA, XM_011543838.4:c.*2002_*2003insACACACACACA, XM_011543838.3:c.*2002_*2003insA, XM_011543838.3:c.*2002_*2003insACA, XM_011543838.3:c.*2002_*2003insACACA, XM_011543838.3:c.*2002_*2003insACACACACACA, XM_011543838.2:c.*2002_*2003insA, XM_011543838.2:c.*2002_*2003insACA, XM_011543838.2:c.*2002_*2003insACACA, XM_011543838.2:c.*2002_*2003insACACACACACA, XM_011543838.1:c.*2002_*2003insA, XM_011543838.1:c.*2002_*2003insACA, XM_011543838.1:c.*2002_*2003insACACA, XM_011543838.1:c.*2002_*2003insACACACACACA, NM_053279.3:c.*2002_*2003insA, NM_053279.3:c.*2002_*2003insACA, NM_053279.3:c.*2002_*2003insACACA, NM_053279.3:c.*2002_*2003insACACACACACA, NM_053279.2:c.*2002_*2003insA, NM_053279.2:c.*2002_*2003insACA, NM_053279.2:c.*2002_*2003insACACA, NM_053279.2:c.*2002_*2003insACACACACACA, XM_011543837.2:c.*2002_*2003insA, XM_011543837.2:c.*2002_*2003insACA, XM_011543837.2:c.*2002_*2003insACACA, XM_011543837.2:c.*2002_*2003insACACACACACA, XM_011543837.1:c.*2002_*2003insA, XM_011543837.1:c.*2002_*2003insACA, XM_011543837.1:c.*2002_*2003insACACA, XM_011543837.1:c.*2002_*2003insACACACACACA, XM_024447292.2:c.*2002_*2003insA, XM_024447292.2:c.*2002_*2003insACA, XM_024447292.2:c.*2002_*2003insACACA, XM_024447292.2:c.*2002_*2003insACACACACACA, XM_024447292.1:c.*2002_*2003insA, XM_024447292.1:c.*2002_*2003insACA, XM_024447292.1:c.*2002_*2003insACACA, XM_024447292.1:c.*2002_*2003insACACACACACA

        4.

        rs1491268634 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          CG>- [Show Flanks]
          Chromosome:
          8:11422355 (GRCh38)
          8:11279864 (GRCh37)
          Canonical SPDI:
          NC_000008.11:11422354:CG:
          Gene:
          FAM167A (Varview), FAM167A-AS1 (Varview)
          Functional Consequence:
          intron_variant,3_prime_UTR_variant
          Validated:
          by frequency,by alfa
          MAF:
          -=0./0 (ALFA)
          -=0.000025/3 (GnomAD)
          HGVS:

          5.

          rs1491208782 has merged into rs57215593 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            GTGTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
            Chromosome:
            8:11422384 (GRCh38)
            8:11279893 (GRCh37)
            Canonical SPDI:
            NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000008.11:11422373:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
            Gene:
            FAM167A (Varview), FAM167A-AS1 (Varview)
            Functional Consequence:
            intron_variant,3_prime_UTR_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            GTGTGTGTGT=0./0 (ALFA)
            -=0.0825/48 (NorthernSweden)
            HGVS:
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NM_053279.3:c.*1968AC[9], NM_053279.3:c.*1968AC[10], NM_053279.3:c.*1968AC[11], NM_053279.3:c.*1968AC[12], NM_053279.3:c.*1968AC[13], NM_053279.3:c.*1968AC[14], NM_053279.3:c.*1968AC[15], NM_053279.3:c.*1968AC[17], NM_053279.3:c.*1968AC[18], NM_053279.3:c.*1968AC[19], NM_053279.3:c.*1968AC[20], NM_053279.3:c.*1968AC[21], NM_053279.3:c.*1968AC[22], NM_053279.3:c.*1968AC[23], NM_053279.3:c.*1968AC[24], NM_053279.3:c.*1968AC[25], NM_053279.3:c.*1968AC[26], NM_053279.2:c.*1968AC[5], NM_053279.2:c.*1968AC[6], NM_053279.2:c.*1968AC[7], NM_053279.2:c.*1968AC[8], NM_053279.2:c.*1968AC[9], NM_053279.2:c.*1968AC[10], NM_053279.2:c.*1968AC[11], NM_053279.2:c.*1968AC[12], NM_053279.2:c.*1968AC[13], NM_053279.2:c.*1968AC[14], NM_053279.2:c.*1968AC[15], NM_053279.2:c.*1968AC[17], NM_053279.2:c.*1968AC[18], NM_053279.2:c.*1968AC[19], NM_053279.2:c.*1968AC[20], NM_053279.2:c.*1968AC[21], NM_053279.2:c.*1968AC[22], NM_053279.2:c.*1968AC[23], NM_053279.2:c.*1968AC[24], NM_053279.2:c.*1968AC[25], NM_053279.2:c.*1968AC[26], XM_011543837.2:c.*1968AC[5], XM_011543837.2:c.*1968AC[6], XM_011543837.2:c.*1968AC[7], XM_011543837.2:c.*1968AC[8], XM_011543837.2:c.*1968AC[9], XM_011543837.2:c.*1968AC[10], XM_011543837.2:c.*1968AC[11], XM_011543837.2:c.*1968AC[12], XM_011543837.2:c.*1968AC[13], XM_011543837.2:c.*1968AC[14], XM_011543837.2:c.*1968AC[15], XM_011543837.2:c.*1968AC[17], XM_011543837.2:c.*1968AC[18], XM_011543837.2:c.*1968AC[19], XM_011543837.2:c.*1968AC[20], XM_011543837.2:c.*1968AC[21], XM_011543837.2:c.*1968AC[22], XM_011543837.2:c.*1968AC[23], XM_011543837.2:c.*1968AC[24], XM_011543837.2:c.*1968AC[25], XM_011543837.2:c.*1968AC[26], XM_011543837.1:c.*1968AC[5], XM_011543837.1:c.*1968AC[6], XM_011543837.1:c.*1968AC[7], XM_011543837.1:c.*1968AC[8], XM_011543837.1:c.*1968AC[9], XM_011543837.1:c.*1968AC[10], XM_011543837.1:c.*1968AC[11], XM_011543837.1:c.*1968AC[12], XM_011543837.1:c.*1968AC[13], XM_011543837.1:c.*1968AC[14], XM_011543837.1:c.*1968AC[15], 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XM_024447292.1:c.*1968AC[7], XM_024447292.1:c.*1968AC[8], XM_024447292.1:c.*1968AC[9], XM_024447292.1:c.*1968AC[10], XM_024447292.1:c.*1968AC[11], XM_024447292.1:c.*1968AC[12], XM_024447292.1:c.*1968AC[13], XM_024447292.1:c.*1968AC[14], XM_024447292.1:c.*1968AC[15], XM_024447292.1:c.*1968AC[17], XM_024447292.1:c.*1968AC[18], XM_024447292.1:c.*1968AC[19], XM_024447292.1:c.*1968AC[20], XM_024447292.1:c.*1968AC[21], XM_024447292.1:c.*1968AC[22], XM_024447292.1:c.*1968AC[23], XM_024447292.1:c.*1968AC[24], XM_024447292.1:c.*1968AC[25], XM_024447292.1:c.*1968AC[26]

            6.

            rs1491171785 has merged into rs1180883138 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              8:11419421 (GRCh38)
              8:11276930 (GRCh37)
              Canonical SPDI:
              NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:11419412:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              FAM167A-AS1 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTT=0./0 (ALFA)
              HGVS:
              NC_000008.11:g.11419421_11419429del, NC_000008.11:g.11419422_11419429del, NC_000008.11:g.11419423_11419429del, NC_000008.11:g.11419424_11419429del, NC_000008.11:g.11419425_11419429del, NC_000008.11:g.11419426_11419429del, NC_000008.11:g.11419427_11419429del, NC_000008.11:g.11419428_11419429del, NC_000008.11:g.11419429del, NC_000008.11:g.11419429dup, NC_000008.11:g.11419428_11419429dup, NC_000008.11:g.11419427_11419429dup, NC_000008.11:g.11419426_11419429dup, NC_000008.11:g.11419425_11419429dup, NC_000008.11:g.11419424_11419429dup, NC_000008.11:g.11419423_11419429dup, NC_000008.11:g.11419422_11419429dup, NC_000008.11:g.11419421_11419429dup, NC_000008.11:g.11419420_11419429dup, NC_000008.11:g.11419417_11419429dup, NC_000008.11:g.11419416_11419429dup, NC_000008.11:g.11419429_11419430insTTTTTTTTTTTTTTTTTTT, NC_000008.11:g.11419429_11419430insTTTTTTTTTTTTTTTTTTTTTTT, NC_000008.10:g.11276930_11276938del, NC_000008.10:g.11276931_11276938del, NC_000008.10:g.11276932_11276938del, NC_000008.10:g.11276933_11276938del, NC_000008.10:g.11276934_11276938del, NC_000008.10:g.11276935_11276938del, NC_000008.10:g.11276936_11276938del, NC_000008.10:g.11276937_11276938del, NC_000008.10:g.11276938del, NC_000008.10:g.11276938dup, NC_000008.10:g.11276937_11276938dup, NC_000008.10:g.11276936_11276938dup, NC_000008.10:g.11276935_11276938dup, NC_000008.10:g.11276934_11276938dup, NC_000008.10:g.11276933_11276938dup, NC_000008.10:g.11276932_11276938dup, NC_000008.10:g.11276931_11276938dup, NC_000008.10:g.11276930_11276938dup, NC_000008.10:g.11276929_11276938dup, NC_000008.10:g.11276926_11276938dup, NC_000008.10:g.11276925_11276938dup, NC_000008.10:g.11276938_11276939insTTTTTTTTTTTTTTTTTTT, NC_000008.10:g.11276938_11276939insTTTTTTTTTTTTTTTTTTTTTTT, NW_018654717.1:g.1929142_1929150del, NW_018654717.1:g.1929143_1929150del, NW_018654717.1:g.1929144_1929150del, NW_018654717.1:g.1929145_1929150del, NW_018654717.1:g.1929146_1929150del, NW_018654717.1:g.1929147_1929150del, NW_018654717.1:g.1929148_1929150del, NW_018654717.1:g.1929149_1929150del, NW_018654717.1:g.1929150del, NW_018654717.1:g.1929150dup, NW_018654717.1:g.1929149_1929150dup, NW_018654717.1:g.1929148_1929150dup, NW_018654717.1:g.1929147_1929150dup, NW_018654717.1:g.1929146_1929150dup, NW_018654717.1:g.1929145_1929150dup, NW_018654717.1:g.1929144_1929150dup, NW_018654717.1:g.1929143_1929150dup, NW_018654717.1:g.1929142_1929150dup, NW_018654717.1:g.1929141_1929150dup, NW_018654717.1:g.1929138_1929150dup, NW_018654717.1:g.1929137_1929150dup, NW_018654717.1:g.1929150_1929151insAAAAAAAAAAAAAAAAAAA, NW_018654717.1:g.1929150_1929151insAAAAAAAAAAAAAAAAAAAAAAA

              7.

              rs1490962581 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>G [Show Flanks]
                Chromosome:
                8:11385626 (GRCh38)
                8:11243135 (GRCh37)
                Canonical SPDI:
                NC_000008.11:11385625:A:G
                Gene:
                FAM167A-AS1 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                G=0./0 (ALFA)
                G=0.000007/1 (GnomAD)
                HGVS:

                8.

                rs1490888030 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>G [Show Flanks]
                  Chromosome:
                  8:11431841 (GRCh38)
                  8:11289350 (GRCh37)
                  Canonical SPDI:
                  NC_000008.11:11431840:T:G
                  Gene:
                  FAM167A (Varview), FAM167A-AS1 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000009/1 (GnomAD)
                  HGVS:

                  9.

                  rs1490883398 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    8:11409561 (GRCh38)
                    8:11267070 (GRCh37)
                    Canonical SPDI:
                    NC_000008.11:11409560:A:G
                    Gene:
                    FAM167A-AS1 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0.000071/1 (ALFA)
                    G=0.000007/1 (GnomAD)
                    G=0.000023/6 (TOPMED)
                    HGVS:

                    10.

                    rs1490857815 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G [Show Flanks]
                      Chromosome:
                      8:11410227 (GRCh38)
                      8:11267736 (GRCh37)
                      Canonical SPDI:
                      NC_000008.11:11410226:A:G
                      Gene:
                      FAM167A-AS1 (Varview)
                      Functional Consequence:
                      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:

                      11.

                      rs1490806660 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>C [Show Flanks]
                        Chromosome:
                        8:11391674 (GRCh38)
                        8:11249183 (GRCh37)
                        Canonical SPDI:
                        NC_000008.11:11391673:A:C
                        Gene:
                        FAM167A-AS1 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000004/1 (TOPMED)
                        C=0.000007/1 (GnomAD)
                        HGVS:

                        12.

                        rs1490798473 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>T [Show Flanks]
                          Chromosome:
                          8:11402072 (GRCh38)
                          8:11259581 (GRCh37)
                          Canonical SPDI:
                          NC_000008.11:11402071:A:T
                          Gene:
                          FAM167A-AS1 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          T=0.00003/8 (TOPMED)
                          T=0.000036/5 (GnomAD)
                          HGVS:

                          13.

                          rs1490788618 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A,C,T [Show Flanks]
                            Chromosome:
                            8:11401216 (GRCh38)
                            8:11258725 (GRCh37)
                            Canonical SPDI:
                            NC_000008.11:11401215:G:A,NC_000008.11:11401215:G:C,NC_000008.11:11401215:G:T
                            Gene:
                            FAM167A-AS1 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            A=0.000007/1 (GnomAD)
                            HGVS:

                            14.

                            rs1490771000 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              8:11387158 (GRCh38)
                              8:11244667 (GRCh37)
                              Canonical SPDI:
                              NC_000008.11:11387157:C:T
                              Gene:
                              FAM167A-AS1 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000004/1 (TOPMED)
                              T=0.000007/1 (GnomAD)
                              HGVS:

                              15.

                              rs1490769364 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>C,G [Show Flanks]
                                Chromosome:
                                8:11421079 (GRCh38)
                                8:11278588 (GRCh37)
                                Canonical SPDI:
                                NC_000008.11:11421078:T:C,NC_000008.11:11421078:T:G
                                Gene:
                                FAM167A (Varview), FAM167A-AS1 (Varview)
                                Functional Consequence:
                                500B_downstream_variant,downstream_transcript_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000036/5 (GnomAD)
                                HGVS:

                                16.

                                rs1490763212 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  8:11400535 (GRCh38)
                                  8:11258044 (GRCh37)
                                  Canonical SPDI:
                                  NC_000008.11:11400534:T:C
                                  Gene:
                                  FAM167A-AS1 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1490727330 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    8:11422615 (GRCh38)
                                    8:11280124 (GRCh37)
                                    Canonical SPDI:
                                    NC_000008.11:11422614:G:T
                                    Gene:
                                    FAM167A (Varview), FAM167A-AS1 (Varview)
                                    Functional Consequence:
                                    intron_variant,3_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000011/3 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1490698451 [Homo sapiens]
                                      Variant type:
                                      DEL
                                      Alleles:
                                      T>- [Show Flanks]
                                      Chromosome:
                                      8:11422387 (GRCh38)
                                      8:11279896 (GRCh37)
                                      Canonical SPDI:
                                      NC_000008.11:11422386:T:
                                      Gene:
                                      FAM167A (Varview), FAM167A-AS1 (Varview)
                                      Functional Consequence:
                                      intron_variant,3_prime_UTR_variant
                                      Validated:
                                      by cluster
                                      HGVS:

                                      19.

                                      rs1490644090 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>A [Show Flanks]
                                        Chromosome:
                                        8:11380616 (GRCh38)
                                        8:11238125 (GRCh37)
                                        Canonical SPDI:
                                        NC_000008.11:11380615:T:A
                                        Gene:
                                        FAM167A-AS1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        A=0./0 (ALFA)
                                        A=0.000004/1 (TOPMED)
                                        A=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1490625637 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>C [Show Flanks]
                                          Chromosome:
                                          8:11401542 (GRCh38)
                                          8:11259051 (GRCh37)
                                          Canonical SPDI:
                                          NC_000008.11:11401541:A:C
                                          Gene:
                                          FAM167A-AS1 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000007/1 (GnomAD)
                                          C=0.000008/2 (TOPMED)
                                          HGVS:

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