| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1A +10 more | |
| | | Duplication (splice acceptor variant) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +10 more | |
| | LMNA, LOC126805877 (A132S +3 more) | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy 1A +10 more | |
| | | Deletion (frameshift variant +2 more) | Dilated cardiomyopathy 1A +10 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Indel (missense variant +1 more) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +12 more | |
| | | Single nucleotide variant (missense variant +2 more) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +11 more | |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +12 more | |
| | | Duplication (frameshift variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (splice acceptor variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Microsatellite (frameshift variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Mandibuloacral dysplasia with type A lipodystrophy +12 more | |
| | | Single nucleotide variant (missense variant) | not specified +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +12 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease type 2 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Primary dilated cardiomyopathy +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 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +12 more | |
| | | Microsatellite (frameshift variant +1 more) | Cardiomyopathy +11 more | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Deletion (inframe_deletion) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +13 more | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | |
| | LMNA, LOC126805877 (R156H +2 more) | Single nucleotide variant (missense variant) | not provided +16 more | |
| | | Single nucleotide variant (missense variant) | Heart-hand syndrome, Slovenian type +12 more | |
| | | Single nucleotide variant (missense variant) | not specified +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Primary dilated cardiomyopathy +12 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +12 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +13 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant +1 more) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (synonymous variant) | Primary dilated cardiomyopathy +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | |
| | LMNA, LOC126805877 (K171E +2 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +13 more | |
| | | Duplication (intron variant) | Charcot-Marie-Tooth disease +13 more | |
| | | Single nucleotide variant (intron variant) | not specified +14 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy +11 more | |
| | | Single nucleotide variant (intron variant) | Emery-Dreifuss muscular dystrophy +9 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules +9 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lethal tight skin contracture syndrome +9 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Lethal tight skin contracture syndrome +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +14 more | |
| | LMNA, LOC126805877 (L25V +2 more) | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +15 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 +11 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +12 more | |
| | | Single nucleotide variant (synonymous variant) | Charcot-Marie-Tooth disease type 2 +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +12 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lethal tight skin contracture syndrome +20 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Familial partial lipodystrophy, Dunnigan type +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Cardiomyopathy +13 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Charcot-Marie-Tooth disease type 2 +13 more | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (intron variant) | not provided +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +14 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Familial partial lipodystrophy, Dunnigan type +11 more | |