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1.

rs4926339 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    1:68456608 (GRCh38)
    1:68922291 (GRCh37)
    Canonical SPDI:
    NC_000001.11:68456607:C:T
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.384539/31946 (ALFA)
    T=0.044248/3426 (TOMMO)
    T=0.045859/134 (KOREAN)
    T=0.047/340 (Korea4K)
    T=0.050764/93 (Korea1K)
    T=0.224641/1125 (1000Genomes)
    T=0.226265/1449 (1000Genomes_30X)
    T=0.23701/447 (HapMap)
    T=0.266795/556 (HGDP_Stanford)
    T=0.273661/1226 (Estonian)
    T=0.316642/83812 (TOPMED)
    T=0.318003/47336 (GnomAD_genomes)
    T=0.336667/202 (NorthernSweden)
    C=0.357759/83 (SGDP_PRJ)
    C=0.375/18 (PRJEB36033)
    T=0.395433/1524 (ALSPAC)
    T=0.402643/1493 (TWINSUK)
    C=0.40625/13 (Siberian)
    T=0.40982/409 (GoNL)
    T=0.449074/97 (Qatari)
    T=0.45/18 (GENOME_DK)
    HGVS:

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