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1.

rs45569333 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A [Show Flanks]
    Chromosome:
    2:233718151 (GRCh38)
    2:234626797 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233718150:T:A
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview)
    Functional Consequence:
    intron_variant,upstream_transcript_variant,2KB_upstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.000071/1 (ALFA)
    A=0.000107/15 (GnomAD)
    A=0.000151/40 (TOPMED)
    A=0.000468/2 (1000Genomes)
    A=0.000684/2 (KOREAN)
    A=0.000885/15 (TOMMO)
    A=0.001092/2 (Korea1K)
    A=0.006944/1 (PharmGKB)
    HGVS:

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