List of variants reported as pathogenic for epilepsy by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001032221.6(STXBP1):c.579-1G>C
NM_001040142.2(SCN2A):c.788C>T (p.Ala263Val)	rs387906686
NM_005898.5(CAPRIN1):c.891_894del (p.Arg297fs)
NM_020708.5(SLC12A5):c.2017C>T (p.Gln673Ter)

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