ClinVar Miner

Submissions for variant NM_000834.5(GRIN2B):c.3796C>T (p.Pro1266Ser)

gnomAD frequency: 0.00004  dbSNP: rs199935748
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000867599 SCV001008845 likely benign Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27 2024-10-28 criteria provided, single submitter clinical testing
New York Genome Center RCV001784473 SCV002025669 uncertain significance Developmental and epileptic encephalopathy, 27 2020-04-28 criteria provided, single submitter clinical testing
GeneDx RCV001785745 SCV002027914 benign not provided 2021-11-21 criteria provided, single submitter clinical testing
Ambry Genetics RCV002352546 SCV002620122 likely benign Inborn genetic diseases 2018-11-15 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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.