List of variants reported as pathogenic for epilepsy by Laboratory of Medical Genetics, University of Torino

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_177550.5(SLC13A5):c.655G>A (p.Gly219Arg)	rs144332569	0.00009
NM_006279.5(ST3GAL3):c.891+1del	rs1387140766
NM_006772.3(SYNGAP1):c.1193del (p.Pro398fs)
NM_014795.4(ZEB2):c.2357dup (p.Leu786fs)

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