List of variants in gene GRIN2D reported as benign for developmental and epileptic encephalopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000836.4(GRIN2D):c.2697T>C (p.Ala899=)	rs62130268	0.81706
NM_000836.4(GRIN2D):c.3142T>C (p.Leu1048=)	rs111420822	0.80040

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