RS58917027 LMNA
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Inborn genetic diseases
Charcot-Marie-Tooth disease type 2
Primary dilated cardiomyopathy
Charcot-Marie-Tooth disease type 2
Cardiovascular phenotype
Dilated cardiomyopathy 1A
Primary dilated cardiomyopathy
Inborn genetic diseases
Charcot-Marie-Tooth disease type 2
Primary dilated cardiomyopathy
Charcot-Marie-Tooth disease type 2
Cardiovascular phenotype
Dilated cardiomyopathy 1A
Other Variants in LMNA