C4013473[trait identifier] AND "Department of Laboratory Medicine, Yon - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1803030	NM_001127644.2(GABRA1):c.84G>T (p.Gln28His)	GABRA1 (Q28H)	Single nucleotide variant (missense variant)	Epilepsy, idiopathic generalized, susceptibility to, 13	GLikely pathogenic
Select item 1803028	NM_001127644.2(GABRA1):c.134T>C (p.Ile45Thr)	GABRA1 (I45T)	Single nucleotide variant (missense variant)	Epilepsy, idiopathic generalized, susceptibility to, 13	GLikely pathogenic