ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1025G>A (p.Arg342Gln)

gnomAD frequency: 0.00069  dbSNP: rs201645096
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
Genetic Services Laboratory, University of Chicago RCV000502237 SCV000597488 likely benign not specified 2020-01-27 criteria provided, single submitter clinical testing
Invitae RCV000903466 SCV001047933 likely benign not provided 2022-12-13 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000502237 SCV001880906 benign not specified 2020-09-18 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.