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1.

rs6817882 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    4:68570517 (GRCh38)
    4:69436235 (GRCh37)
    Canonical SPDI:
    NC_000004.12:68570516:C:T
    Gene:
    UGT2B17 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.432473/5130 (ALFA)
    C=0.107527/20 (SGDP_PRJ)
    C=0.125/3 (Siberian)
    C=0.317073/26 (Vietnamese)
    C=0.34272/1349 (TOMMO)
    C=0.383102/331 (KOREAN)
    T=0.398548/46823 (GnomAD)
    T=0.406152/2034 (1000Genomes)
    C=0.436842/83 (Qatari)
    C=0.452479/219 (Korea1K)
    C=0.461924/461 (GoNL)
    C=0.5/20 (GENOME_DK)
    HGVS:

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