ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.682-13A>G (rs81002888)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breast Cancer Information Core (BIC) (BRCA2) RCV000031650 SCV000147478 uncertain significance Breast-ovarian cancer, familial 2 1999-04-12 no assertion criteria provided clinical testing
Counsyl RCV000031650 SCV000785006 likely benign Breast-ovarian cancer, familial 2 2018-06-13 criteria provided, single submitter clinical testing
GeneDx RCV000608940 SCV000730710 likely benign not specified 2017-11-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000045062 SCV000073075 benign Hereditary breast and ovarian cancer syndrome 2017-06-27 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000031650 SCV000054257 uncertain significance Breast-ovarian cancer, familial 2 2012-01-03 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.