ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.98022C>T (p.Arg32674=) (rs372825562)

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
GeneDx RCV000997340 SCV000528379 likely benign not provided 2021-02-09 criteria provided, single submitter clinical testing
Ambry Genetics RCV000620801 SCV000736844 likely benign Cardiovascular phenotype 2017-06-01 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
CeGaT Praxis fuer Humangenetik Tuebingen RCV000997340 SCV001152623 uncertain significance not provided 2017-03-01 criteria provided, single submitter clinical testing
Invitae RCV001484562 SCV001688981 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-03-26 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.