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Items: 4

1.

rs1333049 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C [Show Flanks]
    Chromosome:
    9:22125504 (GRCh38)
    9:22125503 (GRCh37)
    Canonical SPDI:
    NC_000009.12:22125503:G:A,NC_000009.12:22125503:G:C
    Clinical significance:
    risk-factor
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.468464/1025 (ALFA)
    G=0.318182/14 (Siberian)
    G=0.356784/142 (SGDP_PRJ)
    C=0.381607/722 (HapMap)
    C=0.38257/30106 (PAGE_STUDY)
    C=0.411825/12900 (GnomAD)
    C=0.413919/51975 (TOPMED)
    C=0.418131/2094 (1000Genomes)
    C=0.425/17 (GENOME_DK)
    C=0.439815/95 (Qatari)
    G=0.453704/98 (Vietnamese)
    C=0.455134/2039 (Estonian)
    C=0.46314/1357 (KOREAN)
    C=0.471199/1816 (ALSPAC)
    C=0.471667/283 (NorthernSweden)
    C=0.476954/476 (GoNL)
    G=0.485915/552 (Daghestan)
    C=0.487325/1807 (TWINSUK)
    HGVS:
    NC_000009.12:g.22125504G>A, NC_000009.12:g.22125504G>C, NC_000009.11:g.22125503G>A, NC_000009.11:g.22125503G>C
    2.

    rs59077428 has merged into rs1333049 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A,C [Show Flanks]
      Chromosome:
      9:22125504 (GRCh38)
      9:22125503 (GRCh37)
      Canonical SPDI:
      NC_000009.12:22125503:G:A,NC_000009.12:22125503:G:C
      Clinical significance:
      risk-factor
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.468464/1025 (ALFA)
      G=0.318182/14 (Siberian)
      G=0.356784/142 (SGDP_PRJ)
      C=0.381607/722 (HapMap)
      C=0.38257/30106 (PAGE_STUDY)
      C=0.411825/12900 (GnomAD)
      C=0.413919/51975 (TOPMED)
      C=0.418131/2094 (1000Genomes)
      C=0.425/17 (GENOME_DK)
      C=0.439815/95 (Qatari)
      G=0.453704/98 (Vietnamese)
      C=0.455134/2039 (Estonian)
      C=0.46314/1357 (KOREAN)
      C=0.471199/1816 (ALSPAC)
      C=0.471667/283 (NorthernSweden)
      C=0.476954/476 (GoNL)
      G=0.485915/552 (Daghestan)
      C=0.487325/1807 (TWINSUK)
      HGVS:
      NC_000009.12:g.22125504G>A, NC_000009.12:g.22125504G>C, NC_000009.11:g.22125503G>A, NC_000009.11:g.22125503G>C
      3.

      rs58844516 has merged into rs1333049 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,C [Show Flanks]
        Chromosome:
        9:22125504 (GRCh38)
        9:22125503 (GRCh37)
        Canonical SPDI:
        NC_000009.12:22125503:G:A,NC_000009.12:22125503:G:C
        Clinical significance:
        risk-factor
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        C=0.468464/1025 (ALFA)
        G=0.318182/14 (Siberian)
        G=0.356784/142 (SGDP_PRJ)
        C=0.381607/722 (HapMap)
        C=0.38257/30106 (PAGE_STUDY)
        C=0.411825/12900 (GnomAD)
        C=0.413919/51975 (TOPMED)
        C=0.418131/2094 (1000Genomes)
        C=0.425/17 (GENOME_DK)
        C=0.439815/95 (Qatari)
        G=0.453704/98 (Vietnamese)
        C=0.455134/2039 (Estonian)
        C=0.46314/1357 (KOREAN)
        C=0.471199/1816 (ALSPAC)
        C=0.471667/283 (NorthernSweden)
        C=0.476954/476 (GoNL)
        G=0.485915/552 (Daghestan)
        C=0.487325/1807 (TWINSUK)
        HGVS:
        NC_000009.12:g.22125504G>A, NC_000009.12:g.22125504G>C, NC_000009.11:g.22125503G>A, NC_000009.11:g.22125503G>C
        4.

        rs17761501 has merged into rs1333049 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,C [Show Flanks]
          Chromosome:
          9:22125504 (GRCh38)
          9:22125503 (GRCh37)
          Canonical SPDI:
          NC_000009.12:22125503:G:A,NC_000009.12:22125503:G:C
          Clinical significance:
          risk-factor
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0.468464/1025 (ALFA)
          G=0.318182/14 (Siberian)
          G=0.356784/142 (SGDP_PRJ)
          C=0.381607/722 (HapMap)
          C=0.38257/30106 (PAGE_STUDY)
          C=0.411825/12900 (GnomAD)
          C=0.413919/51975 (TOPMED)
          C=0.418131/2094 (1000Genomes)
          C=0.425/17 (GENOME_DK)
          C=0.439815/95 (Qatari)
          G=0.453704/98 (Vietnamese)
          C=0.455134/2039 (Estonian)
          C=0.46314/1357 (KOREAN)
          C=0.471199/1816 (ALSPAC)
          C=0.471667/283 (NorthernSweden)
          C=0.476954/476 (GoNL)
          G=0.485915/552 (Daghestan)
          C=0.487325/1807 (TWINSUK)
          HGVS:
          NC_000009.12:g.22125504G>A, NC_000009.12:g.22125504G>C, NC_000009.11:g.22125503G>A, NC_000009.11:g.22125503G>C

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