ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.1515G>A (p.Gly505=)

gnomAD frequency: 0.00001  dbSNP: rs753856135
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
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000590539 SCV000697300 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV002530907 SCV003213241 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-06-18 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584667 SCV004359601 likely benign Hereditary cancer-predisposing syndrome 2021-09-01 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.