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1.

rs4557343 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    4:69484288 (GRCh38)
    4:70350006 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69484287:G:A,NC_000004.12:69484287:G:T
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.430325/59112 (ALFA)
    T=0.275/11 (GENOME_DK)
    G=0.295455/13 (Siberian)
    G=0.331658/132 (SGDP_PRJ)
    T=0.369159/79 (Vietnamese)
    T=0.413828/413 (GoNL)
    T=0.418015/1550 (TWINSUK)
    T=0.433835/1672 (ALSPAC)
    T=0.442555/117140 (TOPMED)
    T=0.446667/268 (NorthernSweden)
    T=0.45682/35949 (PAGE_STUDY)
    T=0.467593/101 (Qatari)
    T=0.470276/886 (HapMap)
    T=0.474403/1390 (KOREAN)
    T=0.479258/878 (Korea1K)
    T=0.484072/2424 (1000Genomes)
    T=0.488616/2189 (Estonian)
    T=0.489796/384 (PRJEB37584)
    T=0.496037/8314 (TOMMO)
    HGVS:

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