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1.

rs199473372 [Homo sapiens]
    CACGTGTGTG[G/T]ACATTCGCTG
    Chromosome:
    17:70175271
    Gene:
    KCNJ2 (GeneView)
    Functional Consequence:
    missense
    Allele Origin:
    G(germline)/T(germline)
    Clinical significance:
    untested
    Validated:
    no info
    HGVS:
    NC_000017.10:g.68171412G>T, NC_000017.11:g.70175271G>T, NG_008798.1:g.10737G>T, NM_000891.2:c.232G>T, NP_000882.1:p.Asp78Tyr, XM_005257332.1:c.232G>T, XP_005257389.1:p.Asp78Tyr

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