ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.517-12C>A (rs398122795)

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
Counsyl RCV000077745 SCV000489430 likely benign Breast-ovarian cancer, familial 2 2016-10-05 criteria provided, single submitter clinical testing
Invitae RCV000928268 SCV001073875 likely benign not provided 2018-09-06 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000077745 SCV000109548 uncertain significance Breast-ovarian cancer, familial 2 2008-10-28 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.