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1.

rs6744284 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    2:233716651 (GRCh38)
    2:234625297 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233716650: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=0.316541/66164 (ALFA)
    T=0.065421/14 (Vietnamese)
    T=0.111091/1862 (TOMMO)
    T=0.112658/89 (PRJEB37584)
    T=0.125939/369 (KOREAN)
    T=0.126638/232 (Korea1K)
    T=0.153846/4 (PRJEB36033)
    T=0.270541/270 (GoNL)
    T=0.278857/1034 (TWINSUK)
    T=0.293721/1132 (ALSPAC)
    T=0.295/177 (NorthernSweden)
    T=0.3/12 (GENOME_DK)
    T=0.304515/634 (HGDP_Stanford)
    T=0.313099/196 (Chileans)
    T=0.365741/79 (Qatari)
    C=0.369748/88 (SGDP_PRJ)
    T=0.378564/100202 (TOPMED)
    T=0.383633/53648 (GnomAD)
    T=0.395846/1982 (1000Genomes)
    T=0.400953/757 (HapMap)
    C=0.428571/12 (Siberian)
    HGVS:

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