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1.

rs28675300 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    4:69102440 (GRCh38)
    4:69968158 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69102439:C:G
    Gene:
    UGT2B7 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.031657/598 (ALFA)
    G=0.020766/77 (TWINSUK)
    G=0.021042/21 (GoNL)
    G=0.022321/100 (Estonian)
    G=0.022833/88 (ALSPAC)
    G=0.026667/16 (NorthernSweden)
    G=0.027171/136 (1000Genomes)
    G=0.034261/4801 (GnomAD)
    G=0.035464/9387 (TOPMED)
    G=0.115741/25 (Qatari)
    C=0.46875/15 (SGDP_PRJ)
    C=0.5/2 (Siberian)
    HGVS:

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