"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137521	NM_000834.5(GRIN2B):c.3807A>T (p.Pro1269=)	GRIN2B	Single nucleotide variant (synonymous variant)	GRIN2B-related condition +5 more	GBenign/Likely benign
Select item 246142	NM_000834.5(GRIN2B):c.2481G>A (p.Ala827=)	GRIN2B	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 234500	NM_000834.5(GRIN2B):c.2252T>C (p.Ile751Thr)	GRIN2B (I751T)	Single nucleotide variant (missense variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 245619	NM_000834.5(GRIN2B):c.2172-6G>A	GRIN2B	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 6 +3 more	GLikely benign
Select item 374226	NM_000834.5(GRIN2B):c.2116A>G (p.Met706Val)	GRIN2B (M706V)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 6 +1 more	GLikely pathogenic
Select item 211121	NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=)	GRIN2B	Single nucleotide variant (synonymous variant)	Intellectual disability, autosomal dominant 6 +3 more	GConflicting classifications of pathogenicity
Select item 137515	NM_000834.5(GRIN2B):c.228C>T (p.Thr76=)	GRIN2B	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +4 more	GBenign/Likely benign

ClinVar