List of variants reported as uncertain significance for idiopathic generalized epilepsy by Mendelics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000726.5(CACNB4):c.311G>T (p.Cys104Phe)	rs1805031	0.00074
NM_198904.4(GABRG2):c.1A>G (p.Met1Val)	rs1581275976

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