List of variants reported as pathogenic for generalized epilepsy by 3billion, Medical Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.2575C>T (p.Arg859Cys)	rs121918784
NM_001165963.4(SCN1A):c.2624C>T (p.Thr875Met)	rs121918623
NM_001165963.4(SCN1A):c.2835C>G (p.Phe945Leu)	rs1696628056
NM_052874.5(STX1B):c.733C>T (p.Arg245Ter)	rs780843272

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