List of variants in gene GRIN2B reported as benign by Genetic Services Laboratory, University of Chicago

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000834.5(GRIN2B):c.4218C>T (p.Phe1406=)	rs1805246	0.02603
NM_000834.5(GRIN2B):c.1341C>T (p.Asp447=)	rs35025065	0.00902
NM_000834.5(GRIN2B):c.3498C>T (p.Ser1166=)	rs45600931	0.00538
NM_000834.5(GRIN2B):c.3552C>T (p.Gly1184=)	rs141886903	0.00206
NM_000834.5(GRIN2B):c.1356C>T (p.Tyr452=)	rs142935139	0.00023
NM_000834.5(GRIN2B):c.1780+9G>A	rs201461091	0.00017
NM_000834.5(GRIN2B):c.834C>A (p.Ile278=)	rs199835162	0.00003

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