| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +1 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiac arrest +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Primary familial hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Microsatellite (frameshift variant) | Dilated cardiomyopathy 1BB +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ventricular fibrillation | |