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1.

rs460400 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    6:25053439 (GRCh38)
    6:25053667 (GRCh37)
    Canonical SPDI:
    NC_000006.12:25053438:G:A
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.414981/7839 (ALFA)
    G=0.325137/119 (SGDP_PRJ)
    A=0.330508/78 (HapMap)
    G=0.342105/13 (Siberian)
    A=0.356481/77 (Qatari)
    A=0.372541/98608 (TOPMED)
    A=0.38476/2464 (1000Genomes_30X)
    A=0.391773/1962 (1000Genomes)
    A=0.392722/58474 (GnomAD_genomes)
    A=0.397196/85 (Vietnamese)
    A=0.422937/1630 (ALSPAC)
    A=0.425/17 (GENOME_DK)
    A=0.432309/1603 (TWINSUK)
    A=0.454266/1331 (KOREAN)
    A=0.45491/454 (GoNL)
    A=0.463428/849 (Korea1K)
    A=0.468333/281 (NorthernSweden)
    A=0.474004/3428 (Korea4K)
    A=0.485045/2173 (Estonian)
    G=0.48936/37898 (TOMMO)
    HGVS:

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