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1.

rs1131878 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    4:69480186 (GRCh38)
    4:70345904 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69480185:C:T
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.309219/93689 (ALFA)
    C=0.062036/1040 (TOMMO)
    C=0.080189/17 (Vietnamese)
    C=0.091126/267 (KOREAN)
    C=0.097964/77 (PRJEB37584)
    C=0.116812/214 (Korea1K)
    C=0.148148/8 (Siberian)
    C=0.181102/92 (SGDP_PRJ)
    C=0.216292/77 (PharmGKB)
    C=0.248333/149 (NorthernSweden)
    C=0.252655/1265 (1000Genomes)
    C=0.26317/1179 (Estonian)
    C=0.263717/298 (Daghestan)
    C=0.273016/516 (HapMap)
    C=0.298991/23530 (PAGE_STUDY)
    C=0.314815/68 (Qatari)
    C=0.315558/44163 (GnomAD)
    C=0.315943/83627 (TOPMED)
    C=0.316554/1220 (ALSPAC)
    C=0.328749/1219 (TWINSUK)
    C=0.333667/333 (GoNL)
    C=0.425/17 (GENOME_DK)
    HGVS:

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