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1.

rs5859137 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    C>- [Show Flanks]
    Chromosome:
    4:68667638 (GRCh38)
    4:69533356 (GRCh37)
    Canonical SPDI:
    NC_000004.12:68667637:C:
    Gene:
    UGT2B15 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0./0 (ALFA)
    -=0.019675/99 (1000Genomes)
    -=0.020706/2895 (GnomAD)
    -=0.021247/5624 (TOPMED)
    HGVS:

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