List of variants reported as pathogenic for seizures, benign familial neonatal, 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_172107.4(KCNQ2):c.1687G>A (p.Asp563Asn)	rs796052653
NM_172107.4(KCNQ2):c.620G>A (p.Arg207Gln)	rs118192200
NM_172107.4(KCNQ2):c.638G>A (p.Arg213Gln)
NM_172107.4(KCNQ2):c.917C>T (p.Ala306Val)	rs864321707

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