ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3729A>G (p.Thr1243=) (rs773807182)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162468 SCV000212831 likely benign Hereditary cancer-predisposing syndrome 2015-04-10 criteria provided, single submitter clinical testing
Color RCV000162468 SCV000685437 benign Hereditary cancer-predisposing syndrome 2016-09-12 criteria provided, single submitter clinical testing
Counsyl RCV000663040 SCV000786082 likely benign Hereditary nonpolyposis colorectal cancer type 5 2018-02-20 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000193665 SCV000248076 uncertain significance not specified 2015-06-18 criteria provided, single submitter clinical testing
Invitae RCV000225874 SCV000283819 likely benign Hereditary nonpolyposis colon cancer 2017-12-21 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.