C0282512[trait identifier] AND "Clinical Genetics DNA and cytogenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 205683	NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)	GRIN2A (N1436S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +4 more	GConflicting classifications of pathogenicity
Select item 205693	NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala)	GRIN2A (T1064A)	Single nucleotide variant (missense variant)	Landau-Kleffner syndrome +4 more	GBenign/Likely benign
Select item 205642	NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=)	GRIN2A	Single nucleotide variant (synonymous variant)	GRIN2A-related condition +3 more	GBenign/Likely benign
Select item 129193	NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=)	GRIN2A	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 317666	NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=)	GRIN2A	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 205638	NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met)	GRIN2A (T141M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +4 more	GBenign/Likely benign

ClinVar