"Fulgent Genetics, Fulgent Genetics"[submitter] AND "GRIN2B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 569867	NM_000834.5(GRIN2B):c.4307G>C (p.Gly1436Ala)	GRIN2B (G1436A)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 27 +1 more	GConflicting classifications of pathogenicity
Select item 411106	NM_000834.5(GRIN2B):c.4105G>A (p.Gly1369Ser)	GRIN2B (G1369S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 1023312	NM_000834.5(GRIN2B):c.3647G>A (p.Arg1216His)	GRIN2B (R1216H)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 6 +1 more	GUncertain significance
Select item 245953	NM_000834.5(GRIN2B):c.3549G>A (p.Thr1183=)	GRIN2B	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 595099	NM_000834.5(GRIN2B):c.2845T>C (p.Tyr949His)	GRIN2B (Y949H)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 373655	NM_000834.5(GRIN2B):c.2759G>A (p.Ser920Asn)	GRIN2B (S920N)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 6 +2 more	GUncertain significance
Select item 98436	NM_000834.5(GRIN2B):c.2691C>T (p.Asn897=)	GRIN2B	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign

ClinVar