RS775159300 LMNA
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Associated Conditions
Charcot-Marie-Tooth disease type 2
Hutchinson-Gilford syndrome
Emery-Dreifuss muscular dystrophy
Dilated cardiomyopathy 1A
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Lethal tight skin contracture syndrome
Mandibuloacral dysplasia with type A lipodystrophy
Familial partial lipodystrophy
Other Variants in LMNA