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1.

rs17868335 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A,G,T [Show Flanks]
    Chromosome:
    2:233716337 (GRCh38)
    2:234624983 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233716336:C:A,NC_000002.12:233716336:C:G,NC_000002.12:233716336:C:T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.000061/1 (ALFA)
    A=0.069138/69 (GoNL)
    A=0.084951/315 (TWINSUK)
    A=0.088998/343 (ALSPAC)
    A=0.102932/27245 (TOPMED)
    A=0.12037/26 (Qatari)
    A=0.125/5 (GENOME_DK)
    A=0.13/78 (NorthernSweden)
    A=0.140693/705 (1000Genomes)
    A=0.148805/436 (KOREAN)
    A=0.155568/285 (Korea1K)
    A=0.305556/66 (Vietnamese)
    C=0.443878/87 (SGDP_PRJ)
    C=0.5/8 (Siberian)
    HGVS:

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