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1.

rs199473657 [Homo sapiens]
    GGAAGCTCAT[G/T]TTCGAGCACA
    Chromosome:
    17:70175718
    Gene:
    KCNJ2 (GeneView)
    Functional Consequence:
    missense
    Allele Origin:
    G(germline)/T(germline)
    Clinical significance:
    untested
    Validated:
    no info
    HGVS:
    CM000679.2:g.70175718G>T, NC_000017.10:g.68171859G>T, NC_000017.11:g.70175718G>T, NG_008798.1:g.11184G>T, NM_000891.2:c.679G>T, NP_000882.1:p.Val227Phe, XP_005257389.1:p.Val227Phe

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