RS770579313 TTN

Health Risk Chr 2:178724117
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What This Variant Does
"}} rs770579313, also known as c.21142C&gt
Associated Conditions
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Myopathy
myofibrillar
9
with early respiratory failure
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Myopathy
myofibrillar
9
with early respiratory failure
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
Ask Dr. Hemsworth about this variant