ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3556+13T>C

dbSNP: rs1669884662
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
Color Diagnostics, LLC DBA Color Health RCV001190526 SCV001358030 likely benign Hereditary cancer-predisposing syndrome 2019-01-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465844 SCV002760671 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Invitae RCV002560082 SCV003005692 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-10-05 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.