| | | Single nucleotide variant (missense variant) | Long QT syndrome 3 +8 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +7 more | |
| | | Single nucleotide variant (missense variant) | not specified +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | SUDDEN INFANT DEATH SYNDROME +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 1 +9 more | |
| | LOC110121269, SCN5A (T1016M) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1E +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +12 more | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy 1E +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1E +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Ventricular fibrillation, paroxysmal familial, type 1 +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 3 +9 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |