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Items: 3

1.

rs3940549 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    2:135381057 (GRCh38)
    2:136138627 (GRCh37)
    Canonical SPDI:
    NC_000002.12:135381056:A:G
    Gene:
    ZRANB3 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.495297/20431 (ALFA)
    A=0./0 (Korea1K)
    A=0./0 (TOMMO)
    A=0./0 (Vietnamese)
    A=0.000341/1 (KOREAN)
    A=0.032407/7 (Qatari)
    A=0.05597/30 (SGDP_PRJ)
    A=0.104167/5 (Siberian)
    A=0.163335/818 (1000Genomes)
    G=0.253333/152 (NorthernSweden)
    G=0.286975/1106 (ALSPAC)
    G=0.292585/292 (GoNL)
    G=0.3/12 (GENOME_DK)
    G=0.302589/1122 (TWINSUK)
    A=0.34973/92570 (TOPMED)
    A=0.40008/55988 (GnomAD)
    A=0.484152/2169 (Estonian)
    HGVS:

    2.

    rs4953950 has merged into rs3940549 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      2:135381057 (GRCh38)
      2:136138627 (GRCh37)
      Canonical SPDI:
      NC_000002.12:135381056:A:G
      Gene:
      ZRANB3 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.495297/20431 (ALFA)
      A=0./0 (Korea1K)
      A=0./0 (TOMMO)
      A=0./0 (Vietnamese)
      A=0.000341/1 (KOREAN)
      A=0.032407/7 (Qatari)
      A=0.05597/30 (SGDP_PRJ)
      A=0.104167/5 (Siberian)
      A=0.163335/818 (1000Genomes)
      G=0.253333/152 (NorthernSweden)
      G=0.286975/1106 (ALSPAC)
      G=0.292585/292 (GoNL)
      G=0.3/12 (GENOME_DK)
      G=0.302589/1122 (TWINSUK)
      A=0.34973/92570 (TOPMED)
      A=0.40008/55988 (GnomAD)
      A=0.484152/2169 (Estonian)
      HGVS:

      3.

      rs4283470 has merged into rs3940549 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        2:135381057 (GRCh38)
        2:136138627 (GRCh37)
        Canonical SPDI:
        NC_000002.12:135381056:A:G
        Gene:
        ZRANB3 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.495297/20431 (ALFA)
        A=0./0 (Korea1K)
        A=0./0 (TOMMO)
        A=0./0 (Vietnamese)
        A=0.000341/1 (KOREAN)
        A=0.032407/7 (Qatari)
        A=0.05597/30 (SGDP_PRJ)
        A=0.104167/5 (Siberian)
        A=0.163335/818 (1000Genomes)
        G=0.253333/152 (NorthernSweden)
        G=0.286975/1106 (ALSPAC)
        G=0.292585/292 (GoNL)
        G=0.3/12 (GENOME_DK)
        G=0.302589/1122 (TWINSUK)
        A=0.34973/92570 (TOPMED)
        A=0.40008/55988 (GnomAD)
        A=0.484152/2169 (Estonian)
        HGVS:

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