RS267607632 LMNA
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What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Other Variants in LMNA