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1.

rs10168155 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A,T [Show Flanks]
    Chromosome:
    2:233688190 (GRCh38)
    2:234596836 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233688189:C:A,NC_000002.12:233688189:C:T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.39289/74191 (ALFA)
    T=0.214953/46 (Vietnamese)
    T=0.229352/672 (KOREAN)
    T=0.361649/1811 (1000Genomes)
    T=0.376599/99682 (TOPMED)
    T=0.391304/738 (HapMap)
    C=0.391447/119 (SGDP_PRJ)
    T=0.393217/55037 (GnomAD)
    T=0.397991/1783 (Estonian)
    T=0.398867/1479 (TWINSUK)
    T=0.406667/244 (NorthernSweden)
    T=0.41483/414 (GoNL)
    C=0.416667/15 (Siberian)
    T=0.416667/90 (Qatari)
    T=0.416969/1607 (ALSPAC)
    T=0.45/18 (GENOME_DK)
    HGVS:

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