ClinVar Miner

List of variants in gene KCNQ2 reported as uncertain significance for Benign familial neonatal seizures 1

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Total variants: 2
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NM_172107.3(KCNQ2):c.601C>T (p.Arg201Cys) rs796052623
NM_172107.4(KCNQ2):c.1545G>C (p.Glu515Asp) rs117067974

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