RS59885338 LMNA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2
Autosomal recessive axonal hereditary motor and sensory neuropathy
Hutchinson-Gilford syndrome
Cardiomyopathy
Familial partial lipodystrophy
Dunnigan type
Cardiovascular phenotype
Primary dilated cardiomyopathy
11 conditions
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2
Autosomal recessive axonal hereditary motor and sensory neuropathy
Hutchinson-Gilford syndrome
Cardiomyopathy
Other Variants in LMNA