ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.920+17G>T

dbSNP: rs2080788358
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001185647 SCV001351899 likely benign Hereditary cancer-predisposing syndrome 2019-08-14 criteria provided, single submitter clinical testing
Invitae RCV002068418 SCV002393668 likely benign Peutz-Jeghers syndrome 2023-09-08 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.