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

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004519.4(KCNQ3):c.689G>A (p.Arg230His)	rs749205120
NM_172107.4(KCNQ2):c.1638G>A (p.Met546Ile)	rs2080191127
NM_172107.4(KCNQ2):c.1663T>C (p.Phe555Leu)	rs2145542277
NM_172107.4(KCNQ2):c.388-2A>G	rs2145779858
NM_172107.4(KCNQ2):c.430C>T (p.Arg144Trp)	rs1555873985
NM_172107.4(KCNQ2):c.955A>G (p.Lys319Glu)	rs2145712576

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