List of variants reported as likely pathogenic for epilepsy by Suma Genomics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_177550.5(SLC13A5):c.425C>T (p.Thr142Met)	rs761917087	0.00001
NM_000944.5(PPP3CA):c.530C>G (p.Ala177Gly)	rs2110253722

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