ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8331+14C>T (rs1287378096)

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 RCV000547147 SCV000635659 likely benign Hereditary breast and ovarian cancer syndrome 2017-04-14 criteria provided, single submitter clinical testing
Color RCV000582820 SCV000689114 likely benign Hereditary cancer-predisposing syndrome 2015-08-11 criteria provided, single submitter clinical testing
Counsyl RCV000662863 SCV000785748 likely benign Breast-ovarian cancer, familial 2 2017-11-17 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.