| | | Single nucleotide variant (5 prime UTR variant +1 more) | Familial partial lipodystrophy, Dunnigan type +12 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2 +16 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +12 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +20 more | |
| | | Single nucleotide variant (missense variant) | not provided +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +13 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (synonymous variant) | Heart-hand syndrome, Slovenian type +16 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | not provided +13 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +13 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +14 more | |
| | LMNA, LOC126805877 (R156C +2 more) | Single nucleotide variant (missense variant) | not provided +13 more | |
| | LMNA, LOC126805877 (R156H +2 more) | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +16 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +12 more | GConflicting classifications of pathogenicity |
| | LMNA, LOC126805877 (R166W +2 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | GConflicting classifications of pathogenicity |
| | LMNA, LOC126805877 (R166Q +2 more) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +16 more | GConflicting classifications of pathogenicity |
| | LMNA, LOC126805877 (K171E +2 more) | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +13 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 3, autosomal recessive +20 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (intron variant) | not specified +20 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +15 more | |
| | | Deletion (frameshift variant) | Restrictive dermopathy 2 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +16 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2 +15 more | |
| | | Single nucleotide variant (missense variant) | Familial partial lipodystrophy, Dunnigan type +13 more | |
| | | Single nucleotide variant (nonsense) | Emery-Dreifuss muscular dystrophy 3, autosomal recessive +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +20 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease +20 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Mandibuloacral dysplasia with type A lipodystrophy +12 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (intron variant) | not specified +14 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +16 more | |
| | | Single nucleotide variant (missense variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +12 more | |
| | | Single nucleotide variant (missense variant) | Hutchinson-Gilford syndrome +13 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +15 more | |
| | | Single nucleotide variant (missense variant) | not provided +16 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +16 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 3, autosomal recessive +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (intron variant) | Mandibuloacral dysplasia with type A lipodystrophy +12 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +16 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +14 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial partial lipodystrophy +15 more | |
| | | Single nucleotide variant (missense variant) | Laminopathy +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (synonymous variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +18 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +15 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +12 more | |
| | | Single nucleotide variant (intron variant) | not specified +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +20 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +15 more | |
| | | Single nucleotide variant (splice donor variant) | Charcot-Marie-Tooth disease type 2 +13 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Microsatellite (frameshift variant +1 more) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiomyopathy +13 more | |