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1.

rs1051752 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>G [Show Flanks]
    Chromosome:
    4:69480339 (GRCh38)
    4:70346057 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69480338:T:G
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.016137/948 (ALFA)
    G=0./0 (TWINSUK)
    G=0.001038/4 (ALSPAC)
    G=0.001597/1 (Chileans)
    G=0.00463/1 (Qatari)
    G=0.019886/7 (PharmGKB)
    G=0.033163/4650 (GnomAD)
    G=0.035381/9365 (TOPMED)
    G=0.036696/184 (1000Genomes)
    G=0.049453/3890 (PAGE_STUDY)
    G=0.063291/20 (HapMap)
    T=0.461538/12 (SGDP_PRJ)
    HGVS:

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