List of variants in gene GRIN2A reported as likely benign by Genetic Services Laboratory, University of Chicago

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

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=)	rs2229193
NM_001134407.3(GRIN2A):c.1329-8C>T	rs7193290
NM_001134407.3(GRIN2A):c.1667C>T (p.Ser556Phe)	rs587780349
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=)	rs9806806
NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=)	rs148846694
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=)	rs77705198
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn)	rs540445580
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala)	rs138809301
NM_001134407.3(GRIN2A):c.3246C>G (p.Thr1082=)	rs143039009
NM_001134407.3(GRIN2A):c.3553A>G (p.Lys1185Glu)	rs587780354
NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=)	rs587780350
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=)	rs587780352
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=)	rs367543126
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met)	rs78631453
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile)	rs587780353

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.