| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 3 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Long QT syndrome 3 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +8 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Progressive familial heart block, type 1A +8 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1E +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +8 more | |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Progressive familial heart block, type 1A +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Ventricular fibrillation, paroxysmal familial, type 1 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital long QT syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +8 more | |
| | | Single nucleotide variant (missense variant) | not specified +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 3 +13 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Progressive familial heart block, type 1A +10 more | |
| | | Single nucleotide variant (missense variant) | not specified +10 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +10 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive familial heart block, type 1A +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Progressive familial heart block, type 1A +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Sick sinus syndrome 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Congenital long QT syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1E +5 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1E +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +13 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +10 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital long QT syndrome +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Sick sinus syndrome 1 +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Congenital long QT syndrome +6 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Ventricular fibrillation, paroxysmal familial, type 1 +6 more | |
| | | Single nucleotide variant (synonymous variant) | Ventricular fibrillation, paroxysmal familial, type 1 +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Progressive familial heart block, type 1A +7 more | GConflicting classifications of pathogenicity |