List of variants reported as likely pathogenic for genetic generalized epilepsy by Solve-RD Consortium

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000726.5(CACNB4):c.331G>A (p.Val111Met)	rs764764389	0.00001
NM_052874.5(STX1B):c.160A>T (p.Lys54Ter)	rs2143677745

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