RS779987458 DYSF

Health Risk Chr 2:71665182
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Autosomal recessive limb-girdle muscular dystrophy type 2B
Miyoshi muscular dystrophy 1
Autosomal recessive limb-girdle muscular dystrophy type 2B
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Autosomal recessive limb-girdle muscular dystrophy type 2B
Miyoshi muscular dystrophy 1
Autosomal recessive limb-girdle muscular dystrophy type 2B
Other Variants in DYSF
rs121908953 rs786205081 rs121908955 rs786200896 rs786205082 rs121908956 rs745891180 rs121908957 rs28937581 rs121908958
Ask Dr. Hemsworth about this variant