RS138060032 TTN

Health Risk Chr 2:178799566
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myopathy
myofibrillar
9
with early respiratory failure
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Cardiomyopathy
Early-onset myopathy with fatal cardiomyopathy
Tibial muscular dystrophy
Myopathy
myofibrillar
9
with early respiratory failure
Autosomal recessive limb-girdle muscular dystrophy type 2J
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs587776772 rs199469665
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