List of variants reported as uncertain significance for genetic generalized epilepsy by Centre for Inherited Metabolic Diseases, Karolinska University Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.5735G>A (p.Arg1912Gln)	rs373896263	0.00001
NM_001165963.4(SCN1A):c.4801A>G (p.Thr1601Ala)	rs1573963046

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