| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +1 more | |
| | LOC126807136, ANK2 (T2059M +4 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome +4 more | |
| | ANK2, LOC126807136 (R2069H +4 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene