| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LMNA, LOC126805877 (E161K +2 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 | |
| | | Single nucleotide variant (nonsense) | Dilated cardiomyopathy 1A +5 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (nonsense) | Charcot-Marie-Tooth disease type 2 +1 more | |
Click to view in NCBI Gene