ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2939+6C>T (rs181245759)

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
Counsyl RCV000663279 SCV000786516 uncertain significance Multiple endocrine neoplasia, type 2a 2018-05-16 criteria provided, single submitter clinical testing
Invitae RCV000200761 SCV000255052 uncertain significance Multiple endocrine neoplasia, type 2 2017-10-30 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679739 SCV000807039 likely benign not provided 2017-10-24 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.