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1.

rs35652124 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A,C,G [Show Flanks]
    Chromosome:
    2:177265345 (GRCh38)
    2:178130073 (GRCh37)
    Canonical SPDI:
    NC_000002.12:177265344:T:A,NC_000002.12:177265344:T:C,NC_000002.12:177265344:T:G
    Gene:
    NFE2L2 (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.306898/5944 (ALFA)
    G=0./0 (KOREAN)
    C=0.2/8 (GENOME_DK)
    C=0.243333/146 (NorthernSweden)
    C=0.288023/40352 (GnomAD)
    C=0.29179/77234 (TOPMED)
    T=0.3/12 (Siberian)
    C=0.316073/1172 (TWINSUK)
    C=0.320706/1236 (ALSPAC)
    C=0.325651/325 (GoNL)
    T=0.33631/113 (SGDP_PRJ)
    C=0.341071/1528 (Estonian)
    C=0.375599/1881 (1000Genomes)
    T=0.415811/6969 (TOMMO)
    C=0.416667/90 (Qatari)
    T=0.450328/825 (Korea1K)
    C=0.498731/393 (PRJEB37584)
    HGVS:
    2.

    rs57695243 has merged into rs35652124 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>A,C,G [Show Flanks]
      Chromosome:
      2:177265345 (GRCh38)
      2:178130073 (GRCh37)
      Canonical SPDI:
      NC_000002.12:177265344:T:A,NC_000002.12:177265344:T:C,NC_000002.12:177265344:T:G
      Gene:
      NFE2L2 (Varview)
      Functional Consequence:
      upstream_transcript_variant,2KB_upstream_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.306898/5944 (ALFA)
      G=0./0 (KOREAN)
      C=0.2/8 (GENOME_DK)
      C=0.243333/146 (NorthernSweden)
      C=0.288023/40352 (GnomAD)
      C=0.29179/77234 (TOPMED)
      T=0.3/12 (Siberian)
      C=0.316073/1172 (TWINSUK)
      C=0.320706/1236 (ALSPAC)
      C=0.325651/325 (GoNL)
      T=0.33631/113 (SGDP_PRJ)
      C=0.341071/1528 (Estonian)
      C=0.375599/1881 (1000Genomes)
      T=0.415811/6969 (TOMMO)
      C=0.416667/90 (Qatari)
      T=0.450328/825 (Korea1K)
      C=0.498731/393 (PRJEB37584)
      HGVS:

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