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Items: 2

1.

rs10111905 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    8:97382594 (GRCh38)
    8:98394822 (GRCh37)
    Canonical SPDI:
    NC_000008.11:97382593:T:C
    Gene:
    LOC101927066 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.351666/8888 (ALFA)
    T=0.25/10 (GENOME_DK)
    T=0.259519/259 (GoNL)
    T=0.260045/1165 (Estonian)
    T=0.272472/97 (SGDP_PRJ)
    C=0.277778/60 (Vietnamese)
    T=0.293721/1132 (ALSPAC)
    T=0.299892/1112 (TWINSUK)
    T=0.33/198 (NorthernSweden)
    C=0.377133/1105 (KOREAN)
    C=0.382399/6409 (TOMMO)
    T=0.384615/20 (Siberian)
    T=0.421053/16 (PRJEB36033)
    T=0.436538/61090 (GnomAD)
    T=0.452182/119688 (TOPMED)
    C=0.455671/2282 (1000Genomes)
    C=0.472222/102 (Qatari)
    C=0.472393/154 (HapMap)
    HGVS:
    2.

    rs60211892 has merged into rs10111905 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      8:97382594 (GRCh38)
      8:98394822 (GRCh37)
      Canonical SPDI:
      NC_000008.11:97382593:T:C
      Gene:
      LOC101927066 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.351666/8888 (ALFA)
      T=0.25/10 (GENOME_DK)
      T=0.259519/259 (GoNL)
      T=0.260045/1165 (Estonian)
      T=0.272472/97 (SGDP_PRJ)
      C=0.277778/60 (Vietnamese)
      T=0.293721/1132 (ALSPAC)
      T=0.299892/1112 (TWINSUK)
      T=0.33/198 (NorthernSweden)
      C=0.377133/1105 (KOREAN)
      C=0.382399/6409 (TOMMO)
      T=0.384615/20 (Siberian)
      T=0.421053/16 (PRJEB36033)
      T=0.436538/61090 (GnomAD)
      T=0.452182/119688 (TOPMED)
      C=0.455671/2282 (1000Genomes)
      C=0.472222/102 (Qatari)
      C=0.472393/154 (HapMap)
      HGVS:

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