RS57520892 LMNA
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What This Variant Does
"This is one of the mutations described at *https://www.propublica.org/article/muscular-dystrophy-pat...
Associated Conditions
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Familial partial lipodystrophy
Dunnigan type
Charcot-Marie-Tooth disease type 2
Primary dilated cardiomyopathy
Cardiovascular phenotype
Mandibuloacral dysplasia with type A lipodystrophy
atypical
Mandibuloacral dysplasia
Charcot-Marie-Tooth disease type 2
Cardiomyopathy
Charcot-Marie-Tooth disease
Cardiovascular phenotype
Primary dilated cardiomyopathy
Other Variants in LMNA