List of variants reported as pathogenic for epilepsy by Department of Human Genetics, Hannover Medical School

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001182.5(ALDH7A1):c.695+2T>G
NM_001184880.2(PCDH19):c.2587del (p.Asp862_Leu863insTer)
NM_001367561.1(DOCK7):c.1285C>T (p.Arg429Ter)	rs1057520100

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