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1.

rs853744 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G,T [Show Flanks]
    Chromosome:
    1:213910610 (GRCh38)
    1:214083953 (GRCh37)
    Canonical SPDI:
    NC_000001.11:213910609:A:C,NC_000001.11:213910609:A:G,NC_000001.11:213910609:A:T
    Gene:
    PROX1-AS1 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.016035/527 (ALFA)
    A=0./0 (ALSPAC)
    A=0./0 (GENOME_DK)
    T=0./0 (KOREAN)
    A=0./0 (Korea1K)
    A=0./0 (NorthernSweden)
    A=0./0 (Siberian)
    A=0./0 (TOMMO)
    A=0./0 (TWINSUK)
    A=0./0 (Vietnamese)
    A=0.000223/1 (Estonian)
    A=0.005376/3 (SGDP_PRJ)
    A=0.013889/3 (Qatari)
    A=0.02633/3694 (GnomAD)
    A=0.027957/7400 (TOPMED)
    A=0.029553/148 (1000Genomes)
    A=0.040123/13 (HapMap)
    HGVS:
    2.

    rs57800678 has merged into rs853744 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>C,G,T [Show Flanks]
      Chromosome:
      1:213910610 (GRCh38)
      1:214083953 (GRCh37)
      Canonical SPDI:
      NC_000001.11:213910609:A:C,NC_000001.11:213910609:A:G,NC_000001.11:213910609:A:T
      Gene:
      PROX1-AS1 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.016035/527 (ALFA)
      A=0./0 (ALSPAC)
      A=0./0 (GENOME_DK)
      T=0./0 (KOREAN)
      A=0./0 (Korea1K)
      A=0./0 (NorthernSweden)
      A=0./0 (Siberian)
      A=0./0 (TOMMO)
      A=0./0 (TWINSUK)
      A=0./0 (Vietnamese)
      A=0.000223/1 (Estonian)
      A=0.005376/3 (SGDP_PRJ)
      A=0.013889/3 (Qatari)
      A=0.02633/3694 (GnomAD)
      A=0.027957/7400 (TOPMED)
      A=0.029553/148 (1000Genomes)
      A=0.040123/13 (HapMap)
      HGVS:

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