ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.435A>G (p.Leu145=)

dbSNP: rs2073125482
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
Color Diagnostics, LLC DBA Color Health RCV001182845 SCV001348441 likely benign Cardiomyopathy 2019-01-11 criteria provided, single submitter clinical testing
Ambry Genetics RCV004033081 SCV005018092 likely benign Cardiovascular phenotype 2023-12-10 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
All of Us Research Program, National Institutes of Health RCV004807376 SCV005427568 likely benign Arrhythmogenic right ventricular cardiomyopathy 2024-04-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005093863 SCV005814228 likely benign Arrhythmogenic right ventricular dysplasia 10 2024-07-30 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.