RS368386019 LMNA
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=3
Associated Conditions
Congenital muscular dystrophy
Cardiovascular phenotype
Cardiomyopathy
Charcot-Marie-Tooth disease type 2
Lethal tight skin contracture syndrome
11 conditions
Congenital muscular dystrophy
Cardiovascular phenotype
Cardiomyopathy
Charcot-Marie-Tooth disease type 2
Lethal tight skin contracture syndrome
11 conditions
Other Variants in LMNA