| | | Single nucleotide variant (missense variant +1 more) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | 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) | not provided +12 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Restrictive dermopathy 2 +11 more | |
| | | Deletion (frameshift variant) | Charcot-Marie-Tooth disease type 2 +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +12 more | |
| | | Microsatellite (frameshift variant +1 more) | Charcot-Marie-Tooth disease type 2B1 +11 more | |
| | | Single nucleotide variant (missense variant) | Heart-hand syndrome, Slovenian type +6 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +13 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +13 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +15 more | |
| | LMNA, LOC126805877 (R156H +2 more) | Single nucleotide variant (missense variant) | not specified +16 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +12 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease type 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +1 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +12 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +11 more | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2B1 +13 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +11 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +6 more | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +13 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | LMNA, LOC126805877 (K171E +2 more) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +13 more | |
| | | Duplication (intron variant) | Dilated cardiomyopathy 1A +13 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +10 more | |
| | | Single nucleotide variant (intron variant) | Emery-Dreifuss muscular dystrophy +9 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Emery-Dreifuss muscular dystrophy +9 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Emery-Dreifuss muscular dystrophy +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy +9 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Emery-Dreifuss muscular dystrophy +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial partial lipodystrophy, Dunnigan type +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +13 more | |
| | LMNA, LOC126805877 (L25V +2 more) | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1A +15 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +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) | not provided +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant +4 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +12 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy +20 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +13 more | |
| | | Single nucleotide variant (missense variant +1 more) | Primary dilated cardiomyopathy +13 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiomyopathy +13 more | |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +13 more | GUncertain significance/Uncertain risk allele |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +12 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome +11 more | |
| | LMNA, LOC126805877 (R166W +2 more) | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (missense variant) | Congenital muscular dystrophy due to LMNA mutation +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease type 2 +16 more | |
| | | Single nucleotide variant (missense variant) | Restrictive dermopathy 2 +14 more | |
| | | Single nucleotide variant (missense variant) | Restrictive dermopathy 2 +11 more | |
| | | Single nucleotide variant (missense variant) | Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules +14 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant +1 more) | Restrictive dermopathy 2 +13 more | |
| | | Single nucleotide variant (missense variant) | Restrictive dermopathy 2 +14 more | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +16 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +16 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +15 more | |
| | | Single nucleotide variant (missense variant) | not provided +13 more | |
| | | Single nucleotide variant (synonymous variant) | Emery-Dreifuss muscular dystrophy 3, autosomal recessive +12 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | not specified +15 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +15 more | |
| | | Single nucleotide variant (intron variant) | Emery-Dreifuss muscular dystrophy 3, autosomal recessive +11 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +14 more | |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Microsatellite (inframe_deletion) | Muscular dystrophy | |
| | | Single nucleotide variant (missense variant) | not provided +15 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +16 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +14 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiomyopathy +14 more | |
| | | Single nucleotide variant (intron variant) | not specified +15 more | |
| | | Single nucleotide variant (intron variant) | Charcot-Marie-Tooth disease type 2 +14 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiomyopathy +17 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +16 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Congenital muscular dystrophy due to LMNA mutation +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Emery-Dreifuss muscular dystrophy +16 more | GConflicting classifications of pathogenicity |