ClinVar Miner

Submissions for variant NM_024334.3(TMEM43):c.-6C>T

dbSNP: rs1281893880
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
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000760141 SCV000889929 uncertain significance Hypertrophic cardiomyopathy 2019-03-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003999910 SCV004818070 likely benign Arrhythmogenic right ventricular dysplasia 5 2023-03-09 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.