RS886042618 DMD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Duchenne muscular dystrophy
Progressive muscular dystrophy
Neuromuscular disease caused by qualitative or quantitative defects of dystrophin
Duchenne muscular dystrophy
Progressive muscular dystrophy
Other Variants in DMD