RS398123865 DMD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Duchenne muscular dystrophy
Dilated cardiomyopathy 3B
Becker muscular dystrophy
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Duchenne muscular dystrophy
Dilated cardiomyopathy 3B
Becker muscular dystrophy
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Other Variants in DMD