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Items: 2

1.

rs10882123 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    10:92882737 (GRCh38)
    10:94642494 (GRCh37)
    Canonical SPDI:
    NC_000010.11:92882736:T:C
    Gene:
    EXOC6 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.281682/39969 (ALFA)
    C=0.15/6 (GENOME_DK)
    C=0.239059/33484 (GnomAD)
    C=0.245721/65040 (TOPMED)
    T=0.259259/56 (Vietnamese)
    C=0.275551/275 (GoNL)
    C=0.279241/1251 (Estonian)
    T=0.280568/514 (Korea1K)
    C=0.282304/1088 (ALSPAC)
    T=0.282787/828 (KOREAN)
    C=0.283711/1052 (TWINSUK)
    C=0.296296/64 (Qatari)
    C=0.311667/187 (NorthernSweden)
    T=0.313725/96 (SGDP_PRJ)
    C=0.317653/601 (HapMap)
    T=0.34375/11 (Siberian)
    C=0.376198/1884 (1000Genomes)
    T=0.382697/6414 (TOMMO)
    HGVS:
    2.

    rs17376970 has merged into rs10882123 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      10:92882737 (GRCh38)
      10:94642494 (GRCh37)
      Canonical SPDI:
      NC_000010.11:92882736:T:C
      Gene:
      EXOC6 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.281682/39969 (ALFA)
      C=0.15/6 (GENOME_DK)
      C=0.239059/33484 (GnomAD)
      C=0.245721/65040 (TOPMED)
      T=0.259259/56 (Vietnamese)
      C=0.275551/275 (GoNL)
      C=0.279241/1251 (Estonian)
      T=0.280568/514 (Korea1K)
      C=0.282304/1088 (ALSPAC)
      T=0.282787/828 (KOREAN)
      C=0.283711/1052 (TWINSUK)
      C=0.296296/64 (Qatari)
      C=0.311667/187 (NorthernSweden)
      T=0.313725/96 (SGDP_PRJ)
      C=0.317653/601 (HapMap)
      T=0.34375/11 (Siberian)
      C=0.376198/1884 (1000Genomes)
      T=0.382697/6414 (TOMMO)
      HGVS:

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