RS11575937 LMNA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial partial lipodystrophy
Dunnigan type
Laminopathy
Emery-Dreifuss muscular dystrophy 3
autosomal recessive
Charcot-Marie-Tooth disease type 2
Monogenic diabetes
11 conditions
Cardiomyopathy
Dilated cardiomyopathy 1A
Cardiovascular phenotype
Primary dilated cardiomyopathy
LMNA-related disorder
Lipodystrophy - childhood onset
7 conditions
Other Variants in LMNA