RS373709706 TTN

Health Risk Chr 2:178532093
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Associated Conditions
Inborn genetic diseases
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Myopathy
myofibrillar
9
with early respiratory failure
Cardiovascular phenotype
Early-onset myopathy with fatal cardiomyopathy
Tibial muscular dystrophy
Inborn genetic diseases
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Myopathy
myofibrillar
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
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