ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.943-?_1076+?del

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000076761 SCV000107796 pathogenic Lynch syndrome 2013-09-05 reviewed by expert panel research Large deletion
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000076761 SCV000590994 pathogenic Lynch syndrome 2015-11-20 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.