ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance for History of neurodevelopmental disorder

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_000834.4(GRIN2B):c.1125+5G>A
NM_000834.4(GRIN2B):c.241A>G (p.Ile81Val)
NM_000834.4(GRIN2B):c.2810A>G (p.His937Arg) rs1168893427
NM_000834.4(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968
NM_000834.4(GRIN2B):c.3922G>A (p.Val1308Met) rs374746622
NM_000834.4(GRIN2B):c.3985C>G (p.Arg1329Gly) rs1555101805
NM_000834.4(GRIN2B):c.4066G>A (p.Val1356Met) rs796052579
NM_000834.4(GRIN2B):c.80G>A (p.Arg27His)

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.