ClinVar Miner

Submissions for variant NM_207037.2(TCF12):c.1465A>G (p.Met489Val)

gnomAD frequency: 0.00114  dbSNP: rs149621019
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000889742 SCV001033445 likely benign not provided 2024-03-02 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000889742 SCV003827100 uncertain significance not provided 2019-03-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000889742 SCV005214961 likely benign not provided criteria provided, single submitter not provided

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.