ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1228C>T (p.Gln410Ter) (rs1057515421)

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
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV001256761 SCV001433194 pathogenic Familial hypertrophic cardiomyopathy 1 2019-06-17 criteria provided, single submitter clinical testing
Andelfinger Lab,Centre de Recherche, CHU Sainte Justine RCV000408652 SCV000262693 pathogenic Dilated cardiomyopathy 1A 2015-01-01 no assertion criteria provided research

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.