| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia, ankyrin-B-related +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiac arrhythmia, ankyrin-B-related +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | ANK2, LOC126807136 (T1832I +4 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +2 more | |
| | ANK2, LOC126807136 (H1948Q +4 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia, ankyrin-B-related +1 more | |
| | ANK2, LOC126807136 (K2076N +4 more) | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | ANK2, LOC126807137 (G2293V +4 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | ANK2, LOC126807137 (S2655L +4 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | Cardiac arrhythmia, ankyrin-B-related +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Inversion (missense variant +1 more) | Long QT syndrome +1 more | |