List of variants in gene GRIN2B reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=)	rs77299791	0.00070
NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=)	rs147373250	0.00045
NM_000834.5(GRIN2B):c.3807A>T (p.Pro1269=)	rs78765966	0.00035
NM_000834.5(GRIN2B):c.2481G>A (p.Ala827=)	rs189384622	0.00015
NM_000834.5(GRIN2B):c.2172-6G>A	rs201390691	0.00010

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