ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.738+14C>T

dbSNP: rs374761868
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
Color Diagnostics, LLC DBA Color Health RCV000581449 SCV000691360 likely benign Hereditary cancer-predisposing syndrome 2015-11-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061933 SCV002415582 benign Breast-ovarian cancer, familial, susceptibility to, 4 2023-12-28 criteria provided, single submitter clinical testing
Baylor Genetics RCV002061933 SCV004200406 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 4 2024-03-30 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.