List of variants reported as likely benign for epilepsy by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser)	rs144952836	0.00206
NM_152743.4(BRAT1):c.2041G>A (p.Glu681Lys)	rs145833100	0.00079
NM_001271.4(CHD2):c.3734+20A>G	rs765676490

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