RS1060502639 DMD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Duchenne muscular dystrophy
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Becker muscular dystrophy
Dystrophin deficiency
Cardiomyopathy
Dilated cardiomyopathy 3B
Duchenne muscular dystrophy
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Becker muscular dystrophy
Dystrophin deficiency
Cardiomyopathy
Dilated cardiomyopathy 3B
Other Variants in DMD