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1.

rs45557331 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    2:233635820 (GRCh38)
    2:234544466 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233635819:C:G
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.000139/2 (ALFA)
    G=0.000071/1 (TOMMO)
    G=0.000404/107 (TOPMED)
    G=0.000453/63 (GnomAD)
    G=0.000684/2 (KOREAN)
    G=0.003592/18 (1000Genomes)
    G=0.007463/1 (PharmGKB)
    G=0.041667/9 (Vietnamese)
    HGVS:

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