List of variants reported as uncertain significance for genetic generalized epilepsy by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.1343T>C (p.Ile448Thr)	rs755962326	0.00005
NM_001165963.4(SCN1A):c.5404G>A (p.Glu1802Lys)	rs794726780

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