RS57629361 LMNA
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What This Variant Does
"CLNSIG=5
Associated Conditions
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Hutchinson-Gilford syndrome
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease type 2
Familial partial lipodystrophy
Dunnigan type
Abnormality of the musculature
Congenital muscular dystrophy due to LMNA mutation
Cardiovascular phenotype
Cardiomyopathy
Primary dilated cardiomyopathy
Cardiovascular phenotype
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
Other Variants in LMNA