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1.

rs17863787 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>G [Show Flanks]
    Chromosome:
    2:233702448 (GRCh38)
    2:234611094 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233702447:T:G
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.313283/63485 (ALFA)
    G=0.046729/10 (Vietnamese)
    G=0.098799/181 (Korea1K)
    G=0.098976/290 (KOREAN)
    G=0.0992/1663 (TOMMO)
    G=0.247121/515 (HGDP_Stanford)
    G=0.25/10 (GENOME_DK)
    G=0.259023/488 (HapMap)
    G=0.265147/1328 (1000Genomes)
    G=0.282663/74818 (TOPMED)
    G=0.285714/4 (PRJEB36033)
    G=0.29379/41137 (GnomAD)
    G=0.295591/295 (GoNL)
    G=0.303668/1126 (TWINSUK)
    G=0.31396/1210 (ALSPAC)
    G=0.314815/68 (Qatari)
    G=0.315/189 (NorthernSweden)
    G=0.324777/1455 (Estonian)
    T=0.415/83 (SGDP_PRJ)
    T=0.423077/11 (Siberian)
    HGVS:

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