ClinVar Miner

List of variants in gene DSG2 reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.1945G>A (p.Gly649Ser) rs730880078
NM_001943.5(DSG2):c.2110A>G (p.Ile704Val) rs141388237
NM_001943.5(DSG2):c.2335-7A>G rs528851283
NM_001943.5(DSG2):c.2623A>G (p.Met875Val) rs370316475

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.