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1.

rs17862845 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    2:233625810 (GRCh38)
    2:234534456 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233625809:G:A
    Gene:
    UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa
    MAF:
    A=0.00008/1 (ALFA)
    HGVS:

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