RS112188483 TTN
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
6 conditions
Neuromuscular disease
Cardiovascular phenotype
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
6 conditions
Cardiovascular phenotype
Myopathy
myofibrillar
9
with early respiratory failure
Primary dilated cardiomyopathy
Other Variants in TTN