| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ANK2, LOC126807137 (R2416Q +4 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +3 more | |
| | ANK2, LOC126807137 (R2466H +4 more) | Single nucleotide variant (missense variant +1 more) | not specified +4 more | |
| | ANK2, LOC126807137 (H2486Q +4 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +2 more | GConflicting classifications of pathogenicity |
| | ANK2, LOC126807137 (S2526L +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
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