C2678051[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028874	NM_007325.5(GRIA3):c.69G>A (p.Leu23=)	GRIA3	Single nucleotide variant (synonymous variant)	Syndromic X-linked intellectual disability 94 +1 more	GConflicting classifications of pathogenicity
Select item 1031666	NM_007325.5(GRIA3):c.268+16792G>A	GRIA3 (G139S)	Single nucleotide variant (missense variant +1 more)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 1028873	NM_007325.5(GRIA3):c.1209A>C (p.Glu403Asp)	GRIA3 (E403D)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 561018	NM_007325.5(GRIA3):c.2116A>C (p.Met706Leu)	GRIA3 (M706L)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance
Select item 561019	NM_007325.5(GRIA3):c.2408G>A (p.Gly803Glu)	GRIA3 (G803E)	Single nucleotide variant (missense variant +1 more)	Syndromic X-linked intellectual disability 94 +1 more	GConflicting classifications of pathogenicity
Select item 560997	NM_007325.5(GRIA3):c.2447C>T (p.Thr816Ile)	GRIA3 (T816I)	Single nucleotide variant (missense variant)	Syndromic X-linked intellectual disability 94	GUncertain significance

ClinVar