ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3462G>A (p.Glu1154=)

dbSNP: rs1555556543
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001186057 SCV000739218 likely benign Familial thoracic aortic aneurysm and aortic dissection 2017-07-25 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Color Diagnostics, LLC DBA Color Health RCV001186057 SCV001352395 likely benign Familial thoracic aortic aneurysm and aortic dissection 2019-03-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001398522 SCV001600295 likely benign Aortic aneurysm, familial thoracic 4 2024-12-27 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001186057 SCV004821324 likely benign Familial thoracic aortic aneurysm and aortic dissection 2024-02-22 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.