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1.

rs9309022 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    2:38101063 (GRCh38)
    2:38328205 (GRCh37)
    Canonical SPDI:
    NC_000002.12:38101062:G:A
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.123224/19606 (ALFA)
    A=0.036662/614 (TOMMO)
    A=0.049281/144 (KOREAN)
    A=0.058406/107 (Korea1K)
    A=0.091438/173 (HapMap)
    A=0.1/4 (GENOME_DK)
    A=0.101081/26755 (TOPMED)
    A=0.107728/15092 (GnomAD)
    A=0.108214/542 (1000Genomes)
    A=0.108414/402 (TWINSUK)
    A=0.111667/67 (NorthernSweden)
    A=0.117021/451 (ALSPAC)
    A=0.136273/136 (GoNL)
    A=0.138889/30 (Qatari)
    A=0.139535/12 (PRJEB36033)
    A=0.148936/168 (Daghestan)
    A=0.164062/735 (Estonian)
    G=0.428571/6 (Siberian)
    G=0.432836/58 (SGDP_PRJ)
    HGVS:

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