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1.

rs11902812 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A [Show Flanks]
    Chromosome:
    2:233640242 (GRCh38)
    2:234548888 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233640241:C:A
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.000959/120 (ALFA)
    A=0.004841/24 (1000Genomes)
    A=0.005379/754 (GnomAD)
    A=0.00555/1469 (TOPMED)
    A=0.009259/2 (Qatari)
    A=0.011236/8 (HapMap)
    C=0.5/2 (SGDP_PRJ)
    HGVS:

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