| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +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) | Cardiac arrhythmia +9 more | |
| | LOC110121269, SCN5A (T1016M) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +12 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome 3 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 3 +9 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 3 +8 more | |