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1.

rs1821190 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    4:69494479 (GRCh38)
    4:70360197 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69494478:G:A,NC_000004.12:69494478:G:T
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.00009/8 (ALFA)
    G=0./0 (ALSPAC)
    G=0./0 (GENOME_DK)
    A=0./0 (KOREAN)
    G=0./0 (Korea1K)
    G=0./0 (NorthernSweden)
    G=0./0 (Qatari)
    G=0./0 (SGDP_PRJ)
    G=0./0 (Siberian)
    G=0./0 (TOMMO)
    G=0./0 (TWINSUK)
    G=0./0 (Vietnamese)
    G=0.000107/15 (GnomAD)
    G=0.000125/33 (TOPMED)
    G=0.000156/1 (1000Genomes)
    HGVS:

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