ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.924-13C>T

gnomAD frequency: 0.00979  dbSNP: rs73287544
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001691204 SCV001911680 benign not provided 2019-07-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073247 SCV002375390 benign Neonatal-onset encephalopathy with rigidity and seizures 2025-02-02 criteria provided, single submitter 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.