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1.

rs13128530 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    4:68663530 (GRCh38)
    4:69529248 (GRCh37)
    Canonical SPDI:
    NC_000004.12:68663529:T:C
    Gene:
    UGT2B15 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.229291/4595 (ALFA)
    C=0.137377/2302 (TOMMO)
    C=0.170306/312 (Korea1K)
    C=0.17099/501 (KOREAN)
    C=0.190037/952 (1000Genomes)
    C=0.194444/42 (Qatari)
    C=0.19813/52443 (TOPMED)
    C=0.206405/28895 (GnomAD)
    C=0.25/10 (GENOME_DK)
    C=0.267535/267 (GoNL)
    C=0.277893/1071 (ALSPAC)
    C=0.283981/1053 (TWINSUK)
    C=0.316667/190 (NorthernSweden)
    T=0.375/12 (Siberian)
    T=0.402542/95 (SGDP_PRJ)
    HGVS:

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