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1.

rs7503991 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A [Show Flanks]
    Chromosome:
    17:8908116 (GRCh38)
    17:8811433 (GRCh37)
    Canonical SPDI:
    NC_000017.11:8908115:T:A
    Gene:
    PIK3R5 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency
    MAF:
    A=0./0 (HapMap)
    HGVS:

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