List of variants reported as pathogenic for epilepsy by Laboratory of Functional Genomics, Research Centre for Medical Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.2355-2A>G	rs797044545
NM_001242896.3(DEPDC5):c.3564-1G>C
NM_031844.3(HNRNPU):c.1665_1666del (p.Leu556fs)	rs2102985889

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