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1.

rs2602376 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    2:233673405 (GRCh38)
    2:234582051 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233673404:C:T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.250556/4733 (ALFA)
    T=0.011113/186 (TOMMO)
    T=0.018771/55 (KOREAN)
    T=0.021834/40 (Korea1K)
    T=0.042453/9 (Vietnamese)
    T=0.111111/16 (PharmGKB)
    T=0.131886/249 (HapMap)
    T=0.153654/769 (1000Genomes)
    T=0.182478/377 (HGDP_Stanford)
    T=0.189815/41 (Qatari)
    T=0.192191/50871 (TOPMED)
    T=0.213398/29877 (GnomAD)
    T=0.25/10 (GENOME_DK)
    T=0.286138/1061 (TWINSUK)
    T=0.287054/1286 (Estonian)
    T=0.3/6 (PRJEB36033)
    T=0.300601/300 (GoNL)
    T=0.306954/1183 (ALSPAC)
    T=0.326667/196 (NorthernSweden)
    C=0.440299/59 (SGDP_PRJ)
    C=0.454545/10 (Siberian)
    HGVS:

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