| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LMNA, LOC126805877 (K123del +2 more) | Microsatellite (inframe_deletion) | Primary dilated cardiomyopathy +2 more | |
| | LMNA, LOC126805877 (D126E +2 more) | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy | |
| | LMNA, LOC126805877 (T150A +2 more) | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
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