ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.863-16G>A

gnomAD frequency: 0.00007  dbSNP: rs373096204
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
Color Diagnostics, LLC DBA Color Health RCV000584441 SCV000691557 likely benign Hereditary cancer-predisposing syndrome 2016-09-23 criteria provided, single submitter clinical testing
GeneDx RCV001672888 SCV001889838 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001809685 SCV002057440 likely benign Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing
Invitae RCV001809685 SCV002424528 likely benign Peutz-Jeghers syndrome 2024-01-31 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000584441 SCV002526951 benign Hereditary cancer-predisposing syndrome 2021-09-30 criteria provided, single submitter curation

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.