RS397517889 LMNA
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary dilated cardiomyopathy
Charcot-Marie-Tooth disease type 2
Dilated cardiomyopathy 1A
Charcot-Marie-Tooth disease type 2B1
Cardiovascular phenotype
Congenital muscular dystrophy due to LMNA mutation
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Cardiomyopathy
Primary dilated cardiomyopathy
Charcot-Marie-Tooth disease type 2
Dilated cardiomyopathy 1A
Charcot-Marie-Tooth disease type 2B1
Cardiovascular phenotype
Congenital muscular dystrophy due to LMNA mutation
Other Variants in LMNA