List of variants studied for Epilepsy, childhood absence, susceptibility to, 5; Developmental and epileptic encephalopathy, 43

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_021912.5(GABRB3):c.31C>T (p.Pro11Ser)	rs25409	0.00354
NM_000814.6(GABRB3):c.1269C>G (p.His423Gln)	rs76962261	0.00004
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.969G>A (p.Glu323=)	rs77608123	0.00003
NM_000814.6(GABRB3):c.1042A>G (p.Lys348Glu)
NM_000814.6(GABRB3):c.1081G>A (p.Val361Met)	rs1889329356
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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