List of variants reported as likely pathogenic for seizures, benign familial neonatal, 1 by Génétique des Maladies du Développement, Hospices Civils de Lyon

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_172107.4(KCNQ2):c.1638G>A (p.Met546Ile)	rs2080191127
NM_172107.4(KCNQ2):c.1663T>C (p.Phe555Leu)
NM_172107.4(KCNQ2):c.388-2A>G	rs2145779858
NM_172107.4(KCNQ2):c.430C>T (p.Arg144Trp)
NM_172107.4(KCNQ2):c.955A>G (p.Lys319Glu)	rs2145712576

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