RS368542816 LMNA
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Associated Conditions
Cardiovascular phenotype
Charcot-Marie-Tooth disease type 2
Familial partial lipodystrophy
Dunnigan type
Lethal tight skin contracture syndrome
Hutchinson-Gilford syndrome
Charcot-Marie-Tooth disease type 2B1
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Emery-Dreifuss muscular dystrophy
Mandibuloacral dysplasia with type A lipodystrophy
Dilated cardiomyopathy 1A
Cardiomyopathy
Congenital muscular dystrophy due to LMNA mutation
Lipoatrophy with Diabetes
Other Variants in LMNA