RS398122940 DES

Health Risk Chr 2:219425661
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Abnormality of the musculature
Desmin-related myofibrillar myopathy
Abnormality of the musculature
Desmin-related myofibrillar myopathy
Other Variants in DES
rs59962885 rs121913000 rs60538473 rs121913002 rs57639980 rs121913003 rs57955682 rs121913004 rs58687088 rs121913005
Ask Dr. Hemsworth about this variant