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1.

rs2602366 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>T [Show Flanks]
    Chromosome:
    2:233623738 (GRCh38)
    2:234532384 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233623737:A:T
    Gene:
    UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

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