ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.828+16C>A

gnomAD frequency: 0.22345  dbSNP: rs3737378
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 9
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251707 SCV000308561 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668477 SCV001886589 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002058092 SCV002419421 benign Arrhythmogenic right ventricular dysplasia 10 2024-02-01 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000251707 SCV001740328 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000251707 SCV001923772 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000251707 SCV001929999 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000251707 SCV001956239 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000251707 SCV001965538 benign not specified no assertion criteria provided clinical testing
Cohesion Phenomics RCV003126653 SCV003802736 benign Cardiomyopathy 2022-09-23 no assertion criteria provided 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.