| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806427, TTN (K15136N +5 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
| | LOC126806427, TTN (R15108* +5 more) | Single nucleotide variant (nonsense) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene