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1.

rs6600892 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>T [Show Flanks]
    Chromosome:
    4:69107521 (GRCh38)
    4:69973239 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69107520:A:T
    Gene:
    UGT2B7 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.178772/3377 (ALFA)
    T=0.108333/65 (NorthernSweden)
    T=0.165848/743 (Estonian)
    T=0.179294/691 (ALSPAC)
    T=0.185545/688 (TWINSUK)
    T=0.190325/50377 (TOPMED)
    T=0.194275/27183 (GnomAD)
    T=0.194389/194 (GoNL)
    T=0.203623/1020 (1000Genomes)
    T=0.225/9 (GENOME_DK)
    T=0.236111/51 (Qatari)
    T=0.242904/445 (Korea1K)
    T=0.252901/741 (KOREAN)
    T=0.25798/4324 (TOMMO)
    T=0.29717/63 (Vietnamese)
    A=0.43299/84 (SGDP_PRJ)
    A=0.5/6 (Siberian)
    HGVS:

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