| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (C982R) | Single nucleotide variant (missense variant) | Ventricular fibrillation, paroxysmal familial, type 1 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ventricular fibrillation, paroxysmal familial, type 1 +12 more | |
| | | Single nucleotide variant (missense variant) | Sudden cardiac death | |
| | | Single nucleotide variant (missense variant) | Prolonged QT interval +2 more | |
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