RS886045363 LMNA
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Mandibuloacral dysplasia with type A lipodystrophy
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Familial partial lipodystrophy
Dunnigan type
Emery-Dreifuss muscular dystrophy
Lethal tight skin contracture syndrome
Dilated cardiomyopathy 1A
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Primary dilated cardiomyopathy
Other Variants in LMNA