RS121912496 LMNA
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2
LMNA-related disorder
Laminopathy
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2
LMNA-related disorder
Laminopathy
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Other Variants in LMNA