C5394502[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 440956	NM_001083619.3(GRIA2):c.1831G>A (p.Asp611Asn)	GRIA2 (D611N +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language impairment and behavioral abnormalities	GConflicting classifications of pathogenicity
Select item 1701007	NM_001083619.3(GRIA2):c.2375G>A (p.Gly792Glu)	GRIA2 (G745E +1 more)	Single nucleotide variant (missense variant +1 more)	Neurodevelopmental disorder with language impairment and behavioral abnormalities +1 more	GPathogenic