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1.

rs41297723 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>T [Show Flanks]
    Chromosome:
    4:69483484 (GRCh38)
    4:70349202 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69483483:G:T
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.004081/105 (ALFA)
    T=0.000259/1 (ALSPAC)
    T=0.00027/1 (TWINSUK)
    T=0.00463/1 (Qatari)
    T=0.009292/1302 (GnomAD)
    T=0.009619/2546 (TOPMED)
    T=0.010618/53 (1000Genomes)
    G=0.5/5 (SGDP_PRJ)
    HGVS:

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