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1.

rs35982104 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->T [Show Flanks]
    Chromosome:
    2:233698914 (GRCh38)
    2:234607561 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233698914::T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

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