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Items: 4

1.

rs743507 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G,T [Show Flanks]
    Chromosome:
    7:151010400 (GRCh38)
    7:150707488 (GRCh37)
    Canonical SPDI:
    NC_000007.14:151010399:C:G,NC_000007.14:151010399:C:T
    Gene:
    NOS3 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.247322/51296 (ALFA)
    T=0.123596/66 (MGP)
    C=0.147154/2466 (TOMMO)
    C=0.151515/80 (SGDP_PRJ)
    C=0.159598/715 (Estonian)
    C=0.181667/109 (NorthernSweden)
    C=0.203704/44 (Qatari)
    C=0.206532/430 (HGDP_Stanford)
    C=0.214286/12 (Siberian)
    C=0.21843/640 (KOREAN)
    C=0.224299/48 (Vietnamese)
    C=0.225/9 (GENOME_DK)
    C=0.227037/1137 (1000Genomes)
    C=0.234466/32867 (GnomAD)
    C=0.235955/62455 (TOPMED)
    C=0.237475/237 (GoNL)
    C=0.245484/462 (HapMap)
    C=0.256203/950 (TWINSUK)
    C=0.260768/1005 (ALSPAC)
    C=0.318182/14 (PRJEB36033)
    C=0.361702/34 (PharmGKB)
    HGVS:
    2.

    rs386610132 has merged into rs743507 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G,T [Show Flanks]
      Chromosome:
      7:151010400 (GRCh38)
      7:150707488 (GRCh37)
      Canonical SPDI:
      NC_000007.14:151010399:C:G,NC_000007.14:151010399:C:T
      Gene:
      NOS3 (Varview)
      Functional Consequence:
      genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.247322/51296 (ALFA)
      T=0.123596/66 (MGP)
      C=0.147154/2466 (TOMMO)
      C=0.151515/80 (SGDP_PRJ)
      C=0.159598/715 (Estonian)
      C=0.181667/109 (NorthernSweden)
      C=0.203704/44 (Qatari)
      C=0.206532/430 (HGDP_Stanford)
      C=0.214286/12 (Siberian)
      C=0.21843/640 (KOREAN)
      C=0.224299/48 (Vietnamese)
      C=0.225/9 (GENOME_DK)
      C=0.227037/1137 (1000Genomes)
      C=0.234466/32867 (GnomAD)
      C=0.235955/62455 (TOPMED)
      C=0.237475/237 (GoNL)
      C=0.245484/462 (HapMap)
      C=0.256203/950 (TWINSUK)
      C=0.260768/1005 (ALSPAC)
      C=0.318182/14 (PRJEB36033)
      C=0.361702/34 (PharmGKB)
      HGVS:
      3.

      rs56729499 has merged into rs743507 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>G,T [Show Flanks]
        Chromosome:
        7:151010400 (GRCh38)
        7:150707488 (GRCh37)
        Canonical SPDI:
        NC_000007.14:151010399:C:G,NC_000007.14:151010399:C:T
        Gene:
        NOS3 (Varview)
        Functional Consequence:
        genic_downstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        C=0.247322/51296 (ALFA)
        T=0.123596/66 (MGP)
        C=0.147154/2466 (TOMMO)
        C=0.151515/80 (SGDP_PRJ)
        C=0.159598/715 (Estonian)
        C=0.181667/109 (NorthernSweden)
        C=0.203704/44 (Qatari)
        C=0.206532/430 (HGDP_Stanford)
        C=0.214286/12 (Siberian)
        C=0.21843/640 (KOREAN)
        C=0.224299/48 (Vietnamese)
        C=0.225/9 (GENOME_DK)
        C=0.227037/1137 (1000Genomes)
        C=0.234466/32867 (GnomAD)
        C=0.235955/62455 (TOPMED)
        C=0.237475/237 (GoNL)
        C=0.245484/462 (HapMap)
        C=0.256203/950 (TWINSUK)
        C=0.260768/1005 (ALSPAC)
        C=0.318182/14 (PRJEB36033)
        C=0.361702/34 (PharmGKB)
        HGVS:
        4.

        rs10358805 has merged into rs743507 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>G,T [Show Flanks]
          Chromosome:
          7:151010400 (GRCh38)
          7:150707488 (GRCh37)
          Canonical SPDI:
          NC_000007.14:151010399:C:G,NC_000007.14:151010399:C:T
          Gene:
          NOS3 (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          C=0.247322/51296 (ALFA)
          T=0.123596/66 (MGP)
          C=0.147154/2466 (TOMMO)
          C=0.151515/80 (SGDP_PRJ)
          C=0.159598/715 (Estonian)
          C=0.181667/109 (NorthernSweden)
          C=0.203704/44 (Qatari)
          C=0.206532/430 (HGDP_Stanford)
          C=0.214286/12 (Siberian)
          C=0.21843/640 (KOREAN)
          C=0.224299/48 (Vietnamese)
          C=0.225/9 (GENOME_DK)
          C=0.227037/1137 (1000Genomes)
          C=0.234466/32867 (GnomAD)
          C=0.235955/62455 (TOPMED)
          C=0.237475/237 (GoNL)
          C=0.245484/462 (HapMap)
          C=0.256203/950 (TWINSUK)
          C=0.260768/1005 (ALSPAC)
          C=0.318182/14 (PRJEB36033)
          C=0.361702/34 (PharmGKB)
          HGVS:

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