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1.

rs10199293 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    2:233680858 (GRCh38)
    2:234589504 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233680857:T:C
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    upstream_transcript_variant,intron_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.378761/55534 (ALFA)
    T=0.271493/120 (SGDP_PRJ)
    T=0.296667/178 (NorthernSweden)
    T=0.3/12 (GENOME_DK)
    T=0.3/15 (Siberian)
    T=0.326786/1464 (Estonian)
    T=0.346134/1334 (ALSPAC)
    T=0.352213/49250 (GnomAD)
    T=0.361376/683 (HapMap)
    T=0.371858/98427 (TOPMED)
    C=0.37372/1095 (KOREAN)
    C=0.374717/6280 (TOMMO)
    T=0.377562/1400 (TWINSUK)
    T=0.377756/377 (GoNL)
    T=0.38351/1921 (1000Genomes)
    T=0.402778/87 (Qatari)
    T=0.490385/102 (Vietnamese)
    HGVS:

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