| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Atrial conduction disease | |
| | FPGT-TNNI3K, TNNI3K (L132* +1 more) | Single nucleotide variant (nonsense) | Primary dilated cardiomyopathy | |
| | FPGT-TNNI3K, TNNI3K (I228T +1 more) | Single nucleotide variant (missense variant) | Atrial conduction disease +1 more | |
Click to view in NCBI Gene