ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7617+13C>T

gnomAD frequency: 0.00001  dbSNP: rs776346435
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
Color Diagnostics, LLC DBA Color Health RCV000584269 SCV000689058 likely benign Hereditary cancer-predisposing syndrome 2017-06-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005091500 SCV005816205 likely benign Hereditary breast ovarian cancer syndrome 2024-07-24 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.