List of variants in gene GRIN1 reported as likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.1467+8G>A	rs10747050	0.95319
NM_007327.4(GRIN1):c.789A>G (p.Pro263=)	rs6293	0.23665
NM_007327.4(GRIN1):c.855G>A (p.Val285=)	rs1126442	0.23587
NM_007327.4(GRIN1):c.2241G>C (p.Val747=)	rs116354349	0.01638
NM_007327.4(GRIN1):c.2244G>C (p.Thr748=)	rs79570612	0.01637
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=)	rs116006955	0.00510
NM_007327.4(GRIN1):c.426G>A (p.Pro142=)	rs201424528	0.00003
NM_007327.4(GRIN1):c.2121G>A (p.Glu707=)	rs774389234	0.00001
NM_007327.4(GRIN1):c.357G>A (p.Leu119=)	rs201475721	0.00001
NM_007327.4(GRIN1):c.1701G>A (p.Gly567=)	rs1554770070

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