ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.6532-11G>C

gnomAD frequency: 0.00002  dbSNP: rs372829291
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
GeneDx RCV001703675 SCV000521635 likely benign not provided 2019-06-10 criteria provided, single submitter clinical testing
Counsyl RCV000663240 SCV000786445 likely benign Colorectal cancer, susceptibility to, 12 2018-05-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001703675 SCV002382978 likely benign not provided 2025-01-07 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.