List of variants reported as pathogenic for epilepsy by UCLA Clinical Genomics Center, UCLA

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006772.3(SYNGAP1):c.896del (p.Arg299fs)	rs863224930
NM_020822.3(KCNT1):c.1421G>A (p.Arg474His)
NM_172107.4(KCNQ2):c.841G>T (p.Gly281Trp)	rs794727813

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