List of variants reported as uncertain significance for Epilepsy, childhood absence, susceptibility to, 5; Developmental and epileptic encephalopathy, 43

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000814.6(GABRB3):c.292G>A (p.Ala98Thr)	rs756369937	0.00003
NM_000814.6(GABRB3):c.557C>T (p.Thr186Met)	rs769801846	0.00003
NM_000814.6(GABRB3):c.1042A>G (p.Lys348Glu)
NM_000814.6(GABRB3):c.241-7463G>A
NM_000814.6(GABRB3):c.424C>T (p.Arg142Cys)	rs1892475061
NM_000814.6(GABRB3):c.791C>T (p.Ser264Phe)	rs2140696672

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