| | | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +20 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | LOC126806068, RYR2 (S4377L) | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia +3 more | |
| | C2orf49, FHL2 (F239V +2 more) | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | not provided +7 more | |
| | | Single nucleotide variant (nonsense +1 more) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +1 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +12 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +13 more | |
| | | Single nucleotide variant (intron variant) | Cardiac arrhythmia +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | ANK2, LOC126807137 (R2416Q +4 more) | Single nucleotide variant (missense variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Lethal acantholytic epidermolysis bullosa +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary familial dilated cardiomyopathy +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy with wooly hair and keratoderma +2 more | |
| | | Single nucleotide variant (missense variant) | Lethal acantholytic epidermolysis bullosa +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1JJ +1 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Indel (frameshift variant +1 more) | Dilated cardiomyopathy 1O +5 more | |
| | | Deletion (frameshift variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (splice donor variant +1 more) | Arrhythmogenic right ventricular dysplasia 9 +7 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 9 +4 more | |
| | | Indel (frameshift variant) | Familial isolated arrhythmogenic right ventricular dysplasia +5 more | |
| | | Single nucleotide variant (splice acceptor variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Arrhythmogenic right ventricular dysplasia 9 +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +6 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Arrhythmogenic right ventricular cardiomyopathy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 9 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +3 more | |
| | | Single nucleotide variant (splice donor variant) | Arrhythmogenic right ventricular cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Familial isolated arrhythmogenic right ventricular dysplasia +5 more | |
| | | Single nucleotide variant (missense variant) | Rienhoff syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 12 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Naxos disease +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | JUP-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +2 more | |
| | | Duplication (3 prime UTR variant +1 more) | Familial isolated arrhythmogenic right ventricular dysplasia +6 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_deletion) | Familial isolated arrhythmogenic right ventricular dysplasia +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | DSC2-related disorder +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 11 +5 more | |
| | | Single nucleotide variant (missense variant) | Familial isolated arrhythmogenic right ventricular dysplasia +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | DSG2-related disorder +7 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 cardiomyopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Arrhythmogenic right ventricular cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +4 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 10 +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | DSG2-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Microsatellite (frameshift variant) | Primary dilated cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 19 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Progressive familial heart block type IB +6 more | |
| | | Single nucleotide variant (missense variant) | Duchenne muscular dystrophy +2 more | |
| | | Microsatellite (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |