| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CTF1, LOC130058878 (R176H +1 more) | Single nucleotide variant (missense variant +1 more) | Dilated Cardiomyopathy, Dominant | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Dilated Cardiomyopathy, Dominant | |
| | | Duplication (3 prime UTR variant +1 more) | Dilated Cardiomyopathy, Dominant | |
Click to view in NCBI Gene