"GRIA3-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1653352	NM_007325.5(GRIA3):c.57C>A (p.Val19=)	GRIA3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1347912	NM_007325.5(GRIA3):c.379C>G (p.Pro127Ala)	GRIA3 (P127A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3045288	NM_007325.5(GRIA3):c.999G>A (p.Arg333=)	GRIA3	Single nucleotide variant (synonymous variant)	GRIA3-related condition	GLikely benign
Select item 2631272	NM_007325.5(GRIA3):c.1172G>C (p.Ser391Thr)	GRIA3 (S391T)	Single nucleotide variant (missense variant)	GRIA3-related condition	GUncertain significance
Select item 198752	NM_007325.5(GRIA3):c.1181G>A (p.Arg394Gln)	GRIA3 (R394Q)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94 +4 more	GBenign/Likely benign
Select item 3033585	NM_007325.5(GRIA3):c.1594A>G (p.Ile532Val)	GRIA3 (I532V)	Single nucleotide variant (missense variant)	GRIA3-related condition	GUncertain significance
Select item 1390168	NM_007325.5(GRIA3):c.1771C>T (p.Arg591Cys)	GRIA3 (R591C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3030511	NM_000828.5(GRIA3):c.2396G>T (p.Trp799Leu)	GRIA3 (W799L)	Single nucleotide variant (missense variant +1 more)	GRIA3-related condition	GLikely pathogenic

ClinVar