RS267607608 LMNA
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Associated Conditions
Charcot-Marie-Tooth disease type 2
Congenital muscular dystrophy due to LMNA mutation
Familial partial lipodystrophy
Dunnigan type
Charcot-Marie-Tooth disease type 2
Congenital muscular dystrophy due to LMNA mutation
Familial partial lipodystrophy
Dunnigan type
Other Variants in LMNA