RS397517907 LMNA
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What This Variant Does
"CLNSIG=4
Associated Conditions
Charcot-Marie-Tooth disease type 2
Mandibuloacral dysplasia with type A lipodystrophy
Familial partial lipodystrophy
Dunnigan type
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Emery-Dreifuss muscular dystrophy
Dilated cardiomyopathy 1A
Hutchinson-Gilford syndrome
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Charcot-Marie-Tooth disease type 2B1
Other Variants in LMNA