C3280282[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982912	NM_007327.4(GRIN1):c.711G>A (p.Met237Ile)	GRIN1 (M237I +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GUncertain significance
Select item 1679134	NM_007327.4(GRIN1):c.1664T>C (p.Met555Thr)	GRIN1 (M555T +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GUncertain significance
Select item 976358	NM_007327.4(GRIN1):c.1667A>G (p.Gln556Arg)	GRIN1 (Q556R +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GLikely pathogenic
Select item 975942	NM_007327.4(GRIN1):c.1913G>C (p.Gly638Ala)	GRIN1 (G638A +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GPathogenic/Likely pathogenic
Select item 1329920	NM_007327.4(GRIN1):c.1950C>A (p.Asn650Lys)	GRIN1 (N650K +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GPathogenic
Select item 1284989	NM_007327.4(GRIN1):c.1976G>A (p.Arg659Gln)	GRIN1 (R659Q +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GLikely pathogenic
Select item 3024529	NM_007327.4(GRIN1):c.2015T>C (p.Leu672Pro)	GRIN1 (L672P +1 more)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 8	GUncertain significance

ClinVar