| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 5 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 7, autosomal dominant +7 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | Arrhythmogenic right ventricular dysplasia 5 +2 more | |
| | | Deletion (intron variant) | Cardiomyopathy +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 5 +6 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 5 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 5 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 7, autosomal dominant +4 more | |
| | | Single nucleotide variant (intron variant) | Arrhythmogenic right ventricular dysplasia 5 +2 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 7, autosomal dominant +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +7 more | |
| | | Single nucleotide variant (intron variant) | Arrhythmogenic right ventricular dysplasia 5 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 5 +6 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Arrhythmogenic right ventricular dysplasia 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +7 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 5 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not specified +1 more | |