RS41314035 LMNA
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Associated Conditions
Charcot-Marie-Tooth disease type 2
Mandibuloacral dysplasia with type A lipodystrophy
Lethal tight skin contracture syndrome
Dilated cardiomyopathy 1A
Familial partial lipodystrophy
Dunnigan type
Emery-Dreifuss muscular dystrophy
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Congenital muscular dystrophy due to LMNA mutation
Cardiovascular phenotype
Cardiomyopathy
Emery-Dreifuss muscular dystrophy 2
Other Variants in LMNA