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1.

rs72984479 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    2:233644746 (GRCh38)
    2:234553392 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233644745:G:A
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.004182/79 (ALFA)
    A=0.000312/2 (1000Genomes)
    A=0.001002/1 (GoNL)
    A=0.002308/611 (TOPMED)
    A=0.002427/9 (TWINSUK)
    A=0.002783/390 (GnomAD)
    A=0.004152/16 (ALSPAC)
    A=0.008705/39 (Estonian)
    HGVS:

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