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1.

rs4597901 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    4:69283712 (GRCh38)
    4:70149430 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69283711:A:G
    Gene:
    UGT2B28 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.491814/7991 (ALFA)
    A=0.176471/6 (Siberian)
    A=0.229167/66 (SGDP_PRJ)
    G=0.283654/59 (Qatari)
    A=0.3/12 (GENOME_DK)
    G=0.36649/1835 (1000Genomes)
    G=0.369128/660 (Korea1K)
    G=0.382208/1087 (KOREAN)
    G=0.403846/84 (Vietnamese)
    G=0.414495/6736 (TOMMO)
    G=0.448433/57516 (GnomAD)
    A=0.452906/452 (GoNL)
    HGVS:

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