RS753334568 TTN
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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
6 conditions
Hereditary inclusion-body myopathy
Primary familial dilated cardiomyopathy
Cardiovascular phenotype
Myopathy
myofibrillar
9
with early respiratory failure
Autosomal recessive limb-girdle muscular dystrophy type 2J
Other Variants in TTN