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1.

rs2123622 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C,G [Show Flanks]
    Chromosome:
    2:233651409 (GRCh38)
    2:234560055 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233651408:T:C,NC_000002.12:233651408:T:G
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.000046/1 (ALFA)
    G=0./0 (HapMap)
    C=0.000064/9 (GnomAD)
    C=0.000072/19 (TOPMED)
    C=0.000156/1 (1000Genomes)
    HGVS:

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