"Athena Diagnostics Inc"[submitter] AND "GRIA3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 167157	NM_000828.4(GRIA3):c.-2G=	GRIA3	Duplication (5 prime UTR variant)	Inborn genetic diseases +3 more	GBenign
Select item 129166	NM_007325.5(GRIA3):c.15G>A (p.Lys5=)	GRIA3	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign
Select item 493545	NM_007325.5(GRIA3):c.1166A>C (p.Lys389Thr)	GRIA3 (K389T)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 585951	NM_007325.5(GRIA3):c.1440T>C (p.Tyr480=)	GRIA3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 129168	NM_007325.5(GRIA3):c.1501-8T>A	GRIA3	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1781810	NM_007325.5(GRIA3):c.1878-3T>C	GRIA3	Single nucleotide variant (intron variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 994890	NM_007325.5(GRIA3):c.2552G>A (p.Arg851Gln)	GRIA3 (R851Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar