| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not specified +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | SCN5A-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Conduction disorder of the heart +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 | |
| | | Deletion (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 10 +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +11 more | GConflicting classifications of pathogenicity |
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