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1.

rs1042708 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A [Show Flanks]
    Chromosome:
    2:233693213 (GRCh38)
    2:234601859 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233693212:C:A
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    missense_variant,coding_sequence_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0.006705/7 (HapMap)
    HGVS:

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