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1.

rs702424 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C,T [Show Flanks]
    Chromosome:
    7:122996359 (GRCh38)
    7:122636413 (GRCh37)
    Canonical SPDI:
    NC_000007.14:122996358:G:A,NC_000007.14:122996358:G:C,NC_000007.14:122996358:G:T
    Gene:
    TAS2R16 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    G=0.162037/35 (Qatari)
    G=0.21/105 (SGDP_PRJ)
    G=0.248943/471 (HapMap)
    G=0.25/10 (GENOME_DK)
    G=0.25/12 (Siberian)
    G=0.260097/68845 (TOPMED)
    G=0.27249/40559 (GnomAD_genomes)
    G=0.28045/1796 (1000Genomes_30X)
    G=0.282565/282 (GoNL)
    G=0.286142/1433 (1000Genomes)
    G=0.306694/1182 (ALSPAC)
    G=0.313376/1162 (TWINSUK)
    G=0.356667/214 (NorthernSweden)
    G=0.407589/1826 (Estonian)
    A=0.409524/86 (Vietnamese)
    G=0.419878/3029 (Korea4K)
    G=0.421397/772 (Korea1K)
    G=0.429986/1259 (KOREAN)
    G=0.451126/34928 (TOMMO)
    HGVS:

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