C2678051[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2501003	NM_007325.5(GRIA3):c.783G>A (p.Met261Ile)	GRIA3 (M261I)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 982834	NM_007325.5(GRIA3):c.812A>G (p.Gln271Arg)	GRIA3 (Q271R)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 2501004	NM_007325.5(GRIA3):c.1531A>G (p.Ile511Val)	GRIA3 (I511V)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 2501005	NM_007325.5(GRIA3):c.1581C>A (p.Ser527Arg)	GRIA3 (S527R)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 2500993	NM_007325.5(GRIA3):c.1679T>C (p.Val560Ala)	GRIA3 (V560A)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 2500994	NM_007325.5(GRIA3):c.1957G>T (p.Ala653Ser)	GRIA3 (A653S)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GPathogenic
Select item 2500995	NM_007325.5(GRIA3):c.1973T>C (p.Val658Ala)	GRIA3 (V658A)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GLikely pathogenic

ClinVar