ClinVar Miner

Submissions for variant NM_006231.4(POLE):c.1924-6T>C

gnomAD frequency: 0.00004  dbSNP: rs755311168
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000759265 SCV000556332 likely benign not provided 2024-01-08 criteria provided, single submitter clinical testing
Counsyl RCV000471433 SCV000786549 likely benign Colorectal cancer, susceptibility to, 12 2018-05-22 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759265 SCV000888497 benign not provided 2018-07-11 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.