"OMIM"[submitter] AND "GRIA2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 929839	NM_001083619.3(GRIA2):c.905A>G (p.Asp302Gly)	GRIA2 (D302G +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language impairment and behavioral abnormalities	GLikely pathogenic
Select item 929840	NM_001083619.3(GRIA2):c.1582C>A (p.Pro528Thr)	GRIA2 (P528T +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language impairment and behavioral abnormalities	GLikely pathogenic
Select item 929838	NM_001083619.3(GRIA2):c.1825G>A (p.Gly609Arg)	GRIA2 (G609R +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language impairment and behavioral abnormalities	GLikely pathogenic
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 801356	NM_001083619.3(GRIA2):c.1915G>T (p.Ala639Ser)	GRIA2 (A592S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 929842	NM_001083619.3(GRIA2):c.1939G>C (p.Val647Leu)	GRIA2 (V647L +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with language impairment and behavioral abnormalities	GPathogenic

ClinVar