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1.

rs28969670 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    2:233618914 (GRCh38)
    2:234527560 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233618913:T:C
    Gene:
    UGT1A8 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.001179/17 (ALFA)
    C=0.002083/292 (GnomAD)
    C=0.003899/1032 (TOPMED)
    C=0.015771/79 (1000Genomes)
    C=0.048611/7 (PharmGKB)
    C=0.064199/1076 (TOMMO)
    C=0.066553/195 (KOREAN)
    C=0.068777/126 (Korea1K)
    C=0.074766/16 (Vietnamese)
    T=0.5/1 (Siberian)
    T=0.5/11 (SGDP_PRJ)
    HGVS:

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