RS768345594 TTN
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Cardiovascular phenotype
Primary familial dilated cardiomyopathy
6 conditions
Tibial muscular dystrophy
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Early-onset myopathy with fatal cardiomyopathy
Myopathy
myofibrillar
9
with early respiratory failure
Cardiovascular phenotype
Other Variants in TTN