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1.

rs17862881 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    2:233773434 (GRCh38)
    2:234682080 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233773433:A:G
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A1 (Varview), UGT1A3 (Varview)
    Functional Consequence:
    500B_downstream_variant,downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.011735/1340 (ALFA)
    G=0.000106/2 (TOMMO)
    G=0.000342/1 (KOREAN)
    G=0.008016/8 (GoNL)
    G=0.010937/49 (Estonian)
    G=0.011597/43 (TWINSUK)
    G=0.01263/3343 (TOPMED)
    G=0.013429/67 (1000Genomes)
    G=0.013889/2 (PharmGKB)
    G=0.014008/1965 (GnomAD)
    G=0.014151/3 (Vietnamese)
    G=0.01479/57 (ALSPAC)
    G=0.019027/18 (HapMap)
    G=0.03/18 (NorthernSweden)
    G=0.046296/10 (Qatari)
    G=0.05/2 (GENOME_DK)
    A=0.5/1 (Siberian)
    A=0.5/10 (SGDP_PRJ)
    HGVS:

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