| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene