"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 382825	NM_000814.6(GABRB3):c.682+20A>G	GABRB3	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 445708	NM_000814.6(GABRB3):c.241-20887TA[5]	GABRB3	Microsatellite (intron variant)	not provided	GLikely benign
Select item 377036	NM_000814.6(GABRB3):c.136A>C (p.Lys46Gln)	GABRB3 (K46Q)	Single nucleotide variant (missense variant +1 more)	Epilepsy, childhood absence, susceptibility to, 5 +2 more	GUncertain significance

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