ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.735-9G>C

gnomAD frequency: 0.00003  dbSNP: rs201899557
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001703547 SCV000515770 likely benign not provided 2018-06-11 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000580189 SCV000686685 likely benign Hereditary cancer-predisposing syndrome 2017-06-06 criteria provided, single submitter clinical testing
Invitae RCV000870435 SCV001011932 likely benign Peutz-Jeghers syndrome 2023-10-29 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000870435 SCV004819131 likely benign Peutz-Jeghers syndrome 2023-05-31 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.