ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.345G>A (p.Glu115=)

dbSNP: rs1568858500
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
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000769529 SCV000900924 likely benign Cardiomyopathy 2020-02-14 criteria provided, single submitter clinical testing
Invitae RCV002536606 SCV003250696 likely benign Hypertrophic cardiomyopathy 2022-04-11 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.