RS869312102 TTN

Health Risk Chr 2:178741321
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
Ask Dr. Hemsworth about this variant