| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | KCNE2, LOC105372791 (M23L) | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 4 +3 more | |
| | KCNE2, LOC105372791 (S70N) | Single nucleotide variant (missense variant) | Long QT syndrome 6 +1 more | GConflicting classifications of pathogenicity |
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