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1.

rs3128991 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G,T [Show Flanks]
    Chromosome:
    6:29910609 (GRCh38)
    6:29878386 (GRCh37)
    Canonical SPDI:
    NC_000006.12:29910608:A:G,NC_000006.12:29910608:A:T
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.189765/4472 (ALFA)
    G=0.009112/615 (TOMMO)
    G=0.068765/472 (Korea4K)
    G=0.070508/197 (KOREAN)
    G=0.094276/56 (NorthernSweden)
    G=0.148562/744 (1000Genomes)
    G=0.153498/983 (1000Genomes_30X)
    G=0.154206/33 (Qatari)
    G=0.179769/25542 (GnomAD_genomes)
    G=0.211423/211 (GoNL)
    G=0.225/9 (GENOME_DK)
    A=0.336735/33 (SGDP_PRJ)
    A=0.416667/5 (Siberian)
    HGVS:
    NC_000006.12:g.29910609A>G, NC_000006.12:g.29910609A>T, NC_000006.11:g.29878386A>G, NC_000006.11:g.29878386A>T, NG_016120.1:g.892T>C, NG_016120.1:g.892T>A, NT_113891.3:g.1391991G>A, NT_113891.3:g.1391991G>T, NT_113891.2:g.1392097G>A, NT_113891.2:g.1392097G>T, NT_167248.2:g.1167447A>G, NT_167248.2:g.1167447A>T, NT_167248.1:g.1173043A>G, NT_167248.1:g.1173043A>T, NT_167245.2:g.1167802A>G, NT_167245.2:g.1167802A>T, NT_167245.1:g.1173387A>G, NT_167245.1:g.1173387A>T, NT_167249.2:g.1210336A>G, NT_167249.2:g.1210336A>T, NT_167249.1:g.1209634A>G, NT_167249.1:g.1209634A>T, NT_167246.2:g.1166943A>G, NT_167246.2:g.1166943A>T, NT_167246.1:g.1172563A>G, NT_167246.1:g.1172563A>T, NT_167247.2:g.1167439A>G, NT_167247.2:g.1167439A>T, NT_167247.1:g.1173024A>G, NT_167247.1:g.1173024A>T, NT_167244.2:g.1170317G>A, NT_167244.2:g.1170317G>T, NW_003871063.1:g.146494G>A, NW_003871063.1:g.146494G>T, NT_167244.1:g.1120233G>A, NT_167244.1:g.1120233G>T

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