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Items: 2

1.

rs566806 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    12:91165420 (GRCh38)
    12:91559197 (GRCh37)
    Canonical SPDI:
    NC_000012.12:91165419:G:A,NC_000012.12:91165419:G:T
    Gene:
    DCN (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.293093/20928 (ALFA)
    A=0.175/7 (GENOME_DK)
    A=0.228333/137 (NorthernSweden)
    A=0.229459/229 (GoNL)
    A=0.252009/1129 (Estonian)
    A=0.270227/1002 (TWINSUK)
    A=0.283083/1091 (ALSPAC)
    A=0.324074/70 (Qatari)
    A=0.333333/4 (PRJEB36033)
    G=0.337278/114 (SGDP_PRJ)
    A=0.364994/6117 (TOMMO)
    A=0.3762/784 (HGDP_Stanford)
    A=0.382908/53568 (GnomAD)
    A=0.390476/82 (Vietnamese)
    G=0.4/8 (Siberian)
    A=0.40273/1180 (KOREAN)
    A=0.40331/106752 (TOPMED)
    A=0.414741/2077 (1000Genomes)
    A=0.463376/873 (HapMap)
    HGVS:
    2.

    rs58480920 has merged into rs566806 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A,T [Show Flanks]
      Chromosome:
      12:91165420 (GRCh38)
      12:91559197 (GRCh37)
      Canonical SPDI:
      NC_000012.12:91165419:G:A,NC_000012.12:91165419:G:T
      Gene:
      DCN (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.293093/20928 (ALFA)
      A=0.175/7 (GENOME_DK)
      A=0.228333/137 (NorthernSweden)
      A=0.229459/229 (GoNL)
      A=0.252009/1129 (Estonian)
      A=0.270227/1002 (TWINSUK)
      A=0.283083/1091 (ALSPAC)
      A=0.324074/70 (Qatari)
      A=0.333333/4 (PRJEB36033)
      G=0.337278/114 (SGDP_PRJ)
      A=0.364994/6117 (TOMMO)
      A=0.3762/784 (HGDP_Stanford)
      A=0.382908/53568 (GnomAD)
      A=0.390476/82 (Vietnamese)
      G=0.4/8 (Siberian)
      A=0.40273/1180 (KOREAN)
      A=0.40331/106752 (TOPMED)
      A=0.414741/2077 (1000Genomes)
      A=0.463376/873 (HapMap)
      HGVS:

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