RS142191737 LMNA
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What This Variant Does
"CLNSIG=4
Associated Conditions
Peripheral neuropathy
Charcot-Marie-Tooth disease type 2
Dilated cardiomyopathy 1S
Cardiovascular phenotype
Cardiomyopathy
Hutchinson-Gilford syndrome
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Lethal tight skin contracture syndrome
Dilated cardiomyopathy 1A
Other Variants in LMNA