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1.

rs28946882 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C,G [Show Flanks]
    Chromosome:
    2:233713317 (GRCh38)
    2:234621963 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233713316:A:C,NC_000002.12:233713316:A:G
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant,missense_variant,coding_sequence_variant
    Validated:
    by frequency,by cluster
    MAF:
    C=0./0 (HapMap)
    G=0.000033/4 (ExAC)
    HGVS:

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