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1.

rs35922514 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->C [Show Flanks]
    Chromosome:
    4:68649068 (GRCh38)
    4:69514787 (GRCh37)
    Canonical SPDI:
    NC_000004.12:68649068::C
    Gene:
    UGT2B15 (Varview)
    Functional Consequence:
    intron_variant
    HGVS:

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