ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.852G>A (p.Ala284=) (rs767671540)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000953869 SCV001100465 likely benign not provided 2019-01-09 criteria provided, single submitter clinical testing
Invitae RCV001393986 SCV001595665 likely benign Rigidity and multifocal seizure syndrome, lethal neonatal 2020-04-14 criteria provided, single submitter clinical testing
GeneDx RCV000953869 SCV001801373 likely benign not provided 2018-09-05 no assertion criteria provided clinical testing

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.