RS61672878 LMNA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Muscular dystrophy
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Charcot-Marie-Tooth disease type 2
Sudden unexplained death
Cardiovascular phenotype
Dilated cardiomyopathy 1A
Congenital muscular dystrophy due to LMNA mutation
11 conditions
Charcot-Marie-Tooth disease type 2
Cardiovascular phenotype
Congenital muscular dystrophy due to LMNA mutation
Primary dilated cardiomyopathy
Muscular dystrophy
Emery-Dreifuss muscular dystrophy 2
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