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Items: 7

1.

rs232542 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    2:38101036 (GRCh38)
    2:38328178 (GRCh37)
    Canonical SPDI:
    NC_000002.12:38101035:C:T
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.32878/94728 (ALFA)
    T=0.062327/1045 (TOMMO)
    T=0.069444/15 (Vietnamese)
    T=0.085216/249 (KOREAN)
    T=0.097162/178 (Korea1K)
    T=0.108586/86 (PRJEB37584)
    T=0.275/11 (GENOME_DK)
    T=0.291964/1308 (Estonian)
    T=0.295/177 (NorthernSweden)
    T=0.300864/627 (HGDP_Stanford)
    T=0.302589/1122 (TWINSUK)
    T=0.315257/1215 (ALSPAC)
    T=0.336977/1688 (1000Genomes)
    T=0.340681/340 (GoNL)
    T=0.363347/686 (HapMap)
    T=0.371009/51873 (GnomAD)
    T=0.371144/98238 (TOPMED)
    C=0.380165/92 (SGDP_PRJ)
    T=0.381655/29866 (PAGE_STUDY)
    T=0.425926/92 (Qatari)
    C=0.444444/8 (Siberian)
    C=0.5/46 (PRJEB36033)
    HGVS:

    PubMed

    2.

    rs386564970 has merged into rs232542 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      2:38101036 (GRCh38)
      2:38328178 (GRCh37)
      Canonical SPDI:
      NC_000002.12:38101035:C:T
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0.32878/94728 (ALFA)
      T=0.062327/1045 (TOMMO)
      T=0.069444/15 (Vietnamese)
      T=0.085216/249 (KOREAN)
      T=0.097162/178 (Korea1K)
      T=0.108586/86 (PRJEB37584)
      T=0.275/11 (GENOME_DK)
      T=0.291964/1308 (Estonian)
      T=0.295/177 (NorthernSweden)
      T=0.300864/627 (HGDP_Stanford)
      T=0.302589/1122 (TWINSUK)
      T=0.315257/1215 (ALSPAC)
      T=0.336977/1688 (1000Genomes)
      T=0.340681/340 (GoNL)
      T=0.363347/686 (HapMap)
      T=0.371009/51873 (GnomAD)
      T=0.371144/98238 (TOPMED)
      C=0.380165/92 (SGDP_PRJ)
      T=0.381655/29866 (PAGE_STUDY)
      T=0.425926/92 (Qatari)
      C=0.444444/8 (Siberian)
      C=0.5/46 (PRJEB36033)
      HGVS:

      3.

      rs58394523 has merged into rs232542 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>T [Show Flanks]
        Chromosome:
        2:38101036 (GRCh38)
        2:38328178 (GRCh37)
        Canonical SPDI:
        NC_000002.12:38101035:C:T
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.32878/94728 (ALFA)
        T=0.062327/1045 (TOMMO)
        T=0.069444/15 (Vietnamese)
        T=0.085216/249 (KOREAN)
        T=0.097162/178 (Korea1K)
        T=0.108586/86 (PRJEB37584)
        T=0.275/11 (GENOME_DK)
        T=0.291964/1308 (Estonian)
        T=0.295/177 (NorthernSweden)
        T=0.300864/627 (HGDP_Stanford)
        T=0.302589/1122 (TWINSUK)
        T=0.315257/1215 (ALSPAC)
        T=0.336977/1688 (1000Genomes)
        T=0.340681/340 (GoNL)
        T=0.363347/686 (HapMap)
        T=0.371009/51873 (GnomAD)
        T=0.371144/98238 (TOPMED)
        C=0.380165/92 (SGDP_PRJ)
        T=0.381655/29866 (PAGE_STUDY)
        T=0.425926/92 (Qatari)
        C=0.444444/8 (Siberian)
        C=0.5/46 (PRJEB36033)
        HGVS:

        4.

        rs17021980 has merged into rs232542 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          2:38101036 (GRCh38)
          2:38328178 (GRCh37)
          Canonical SPDI:
          NC_000002.12:38101035:C:T
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0.32878/94728 (ALFA)
          T=0.062327/1045 (TOMMO)
          T=0.069444/15 (Vietnamese)
          T=0.085216/249 (KOREAN)
          T=0.097162/178 (Korea1K)
          T=0.108586/86 (PRJEB37584)
          T=0.275/11 (GENOME_DK)
          T=0.291964/1308 (Estonian)
          T=0.295/177 (NorthernSweden)
          T=0.300864/627 (HGDP_Stanford)
          T=0.302589/1122 (TWINSUK)
          T=0.315257/1215 (ALSPAC)
          T=0.336977/1688 (1000Genomes)
          T=0.340681/340 (GoNL)
          T=0.363347/686 (HapMap)
          T=0.371009/51873 (GnomAD)
          T=0.371144/98238 (TOPMED)
          C=0.380165/92 (SGDP_PRJ)
          T=0.381655/29866 (PAGE_STUDY)
          T=0.425926/92 (Qatari)
          C=0.444444/8 (Siberian)
          C=0.5/46 (PRJEB36033)
          HGVS:

          5.

          rs13031277 has merged into rs232542 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            2:38101036 (GRCh38)
            2:38328178 (GRCh37)
            Canonical SPDI:
            NC_000002.12:38101035:C:T
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            T=0.32878/94728 (ALFA)
            T=0.062327/1045 (TOMMO)
            T=0.069444/15 (Vietnamese)
            T=0.085216/249 (KOREAN)
            T=0.097162/178 (Korea1K)
            T=0.108586/86 (PRJEB37584)
            T=0.275/11 (GENOME_DK)
            T=0.291964/1308 (Estonian)
            T=0.295/177 (NorthernSweden)
            T=0.300864/627 (HGDP_Stanford)
            T=0.302589/1122 (TWINSUK)
            T=0.315257/1215 (ALSPAC)
            T=0.336977/1688 (1000Genomes)
            T=0.340681/340 (GoNL)
            T=0.363347/686 (HapMap)
            T=0.371009/51873 (GnomAD)
            T=0.371144/98238 (TOPMED)
            C=0.380165/92 (SGDP_PRJ)
            T=0.381655/29866 (PAGE_STUDY)
            T=0.425926/92 (Qatari)
            C=0.444444/8 (Siberian)
            C=0.5/46 (PRJEB36033)
            HGVS:

            6.

            rs467324 has merged into rs232542 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              2:38101036 (GRCh38)
              2:38328178 (GRCh37)
              Canonical SPDI:
              NC_000002.12:38101035:C:T
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0.32878/94728 (ALFA)
              T=0.062327/1045 (TOMMO)
              T=0.069444/15 (Vietnamese)
              T=0.085216/249 (KOREAN)
              T=0.097162/178 (Korea1K)
              T=0.108586/86 (PRJEB37584)
              T=0.275/11 (GENOME_DK)
              T=0.291964/1308 (Estonian)
              T=0.295/177 (NorthernSweden)
              T=0.300864/627 (HGDP_Stanford)
              T=0.302589/1122 (TWINSUK)
              T=0.315257/1215 (ALSPAC)
              T=0.336977/1688 (1000Genomes)
              T=0.340681/340 (GoNL)
              T=0.363347/686 (HapMap)
              T=0.371009/51873 (GnomAD)
              T=0.371144/98238 (TOPMED)
              C=0.380165/92 (SGDP_PRJ)
              T=0.381655/29866 (PAGE_STUDY)
              T=0.425926/92 (Qatari)
              C=0.444444/8 (Siberian)
              C=0.5/46 (PRJEB36033)
              HGVS:

              7.

              rs234557 has merged into rs232542 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                2:38101036 (GRCh38)
                2:38328178 (GRCh37)
                Canonical SPDI:
                NC_000002.12:38101035:C:T
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0.32878/94728 (ALFA)
                T=0.062327/1045 (TOMMO)
                T=0.069444/15 (Vietnamese)
                T=0.085216/249 (KOREAN)
                T=0.097162/178 (Korea1K)
                T=0.108586/86 (PRJEB37584)
                T=0.275/11 (GENOME_DK)
                T=0.291964/1308 (Estonian)
                T=0.295/177 (NorthernSweden)
                T=0.300864/627 (HGDP_Stanford)
                T=0.302589/1122 (TWINSUK)
                T=0.315257/1215 (ALSPAC)
                T=0.336977/1688 (1000Genomes)
                T=0.340681/340 (GoNL)
                T=0.363347/686 (HapMap)
                T=0.371009/51873 (GnomAD)
                T=0.371144/98238 (TOPMED)
                C=0.380165/92 (SGDP_PRJ)
                T=0.381655/29866 (PAGE_STUDY)
                T=0.425926/92 (Qatari)
                C=0.444444/8 (Siberian)
                C=0.5/46 (PRJEB36033)
                HGVS:

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