ClinVar Miner

Submissions for variant NM_002878.3(RAD51D):c.979C>T (p.Gln327Ter) (rs786203974)

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
Ambry Genetics RCV000167509 SCV000218367 uncertain significance Hereditary cancer-predisposing syndrome 2014-12-31 criteria provided, single submitter clinical testing Insufficient or inconclusive evidence
PreventionGenetics,PreventionGenetics RCV000679544 SCV000806592 uncertain significance not provided 2016-12-20 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.