ClinVar Miner

Submissions for variant MHS6:c.3647-65_3647-61del

dbSNP: rs3136363
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
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000030270 SCV000052937 uncertain Lynch syndrome 2011-08-18 criteria provided, single submitter curation Converted during submission to Uncertain significance.
Invitae RCV001518389 SCV001727067 benign Hereditary nonpolyposis colorectal neoplasms 2022-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001588832 SCV001826747 likely benign not provided 2019-11-09 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 10786688, 30238922)
Sema4, Sema4 RCV002256009 SCV002528052 benign Hereditary cancer-predisposing syndrome 2020-07-28 criteria provided, single submitter curation
CeGaT Center for Human Genetics Tuebingen RCV001588832 SCV003916108 likely benign not provided 2023-09-01 criteria provided, single submitter clinical testing MSH6: BP4, BS1

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.