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1.

rs11488583 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    1:199747846 (GRCh38)
    1:199716974 (GRCh37)
    Canonical SPDI:
    NC_000001.11:199747845:G:A
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.410763/13266 (ALFA)
    G=0.323529/11 (Siberian)
    G=0.353591/128 (SGDP_PRJ)
    A=0.353774/75 (Vietnamese)
    A=0.375/15 (GENOME_DK)
    A=0.393339/104113 (TOPMED)
    A=0.397246/750 (HapMap)
    A=0.397804/59163 (GnomAD_genomes)
    A=0.401747/736 (Korea1K)
    A=0.402009/1801 (Estonian)
    A=0.403342/2583 (1000Genomes_30X)
    A=0.403355/2020 (1000Genomes)
    A=0.407407/88 (Qatari)
    A=0.407816/407 (GoNL)
    A=0.416897/3015 (Korea4K)
    A=0.425566/1578 (TWINSUK)
    A=0.429165/1654 (ALSPAC)
    A=0.438525/1284 (KOREAN)
    A=0.465484/36048 (TOMMO)
    A=0.498333/299 (NorthernSweden)
    HGVS:

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