| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | TTN, TTN-AS1 (K26600fs +5 more) | Deletion (frameshift variant) | Abnormality of the musculature | |
| | TTN, TTN-AS1 (S12114G +5 more) | Single nucleotide variant (missense variant) | Congenital myopathy +1 more | |
Click to view in NCBI Gene