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1.

rs2736445 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    4:69479890 (GRCh38)
    4:70345608 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69479889:A:G
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    500B_downstream_variant,downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.00001/1 (ALFA)
    G=0./0 (HapMap)
    HGVS:

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