RS60890628 LMNA
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Dilated cardiomyopathy 1A
Mandibuloacral dysplasia with type A lipodystrophy
atypical
Familial partial lipodystrophy
Dunnigan type
Cardiovascular phenotype
Charcot-Marie-Tooth disease type 2
Cardiomyopathy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
11 conditions
Dilated cardiomyopathy 1A
Mandibuloacral dysplasia with type A lipodystrophy
atypical
Familial partial lipodystrophy
Other Variants in LMNA