"Fulgent Genetics, Fulgent Genetics"[submitter] AND "GABRG2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 581040	NM_198904.4(GABRG2):c.353C>T (p.Ala118Val)	GABRG2 (A118V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 205553	NM_198904.4(GABRG2):c.1112A>C (p.Lys371Thr)	GABRG2 (K371T +8 more)	Single nucleotide variant (missense variant +1 more)	Febrile seizures, familial, 8 +2 more	GUncertain significance