C1969810[trait identifier] AND "MGZ Medical Genetics Center"[submitter - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1709680	NM_198904.4(GABRG2):c.247C>A (p.Pro83Thr)	GABRG2 (P54T +3 more)	Single nucleotide variant (missense variant +1 more)	Febrile seizures, familial, 8 +1 more	GConflicting classifications of pathogenicity
Select item 1709991	NM_198904.4(GABRG2):c.941C>A (p.Thr314Lys)	GABRG2 (T174K +8 more)	Single nucleotide variant (missense variant +1 more)	Febrile seizures, familial, 8 +1 more	GConflicting classifications of pathogenicity