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1.

rs4485562 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    2:233688920 (GRCh38)
    2:234597566 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233688919:G:A,NC_000002.12:233688919:G:T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.205958/18044 (ALFA)
    A=0.087859/55 (Chileans)
    A=0.118205/1981 (TOMMO)
    A=0.12037/26 (Qatari)
    A=0.145392/426 (KOREAN)
    A=0.149563/274 (Korea1K)
    A=0.170675/855 (1000Genomes)
    A=0.175107/46349 (TOPMED)
    A=0.181014/25355 (GnomAD)
    A=0.184261/384 (HGDP_Stanford)
    A=0.207415/207 (GoNL)
    A=0.222762/826 (TWINSUK)
    A=0.237156/914 (ALSPAC)
    A=0.23913/22 (PRJEB36033)
    A=0.25/10 (GENOME_DK)
    A=0.274777/1231 (Estonian)
    A=0.283019/60 (Vietnamese)
    A=0.296667/178 (NorthernSweden)
    G=0.416667/10 (Siberian)
    G=0.434343/86 (SGDP_PRJ)
    HGVS:

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