RS72648263 TTN
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What This Variant Does
"CLNSIG=3
Associated Conditions
Tibial muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Early-onset myopathy with fatal cardiomyopathy
Dilated cardiomyopathy 1G
Myopathy
myofibrillar
9
with early respiratory failure
Cardiovascular phenotype
Cardiomyopathy
Ventricular fibrillation
TTN-related disorder
Tibial muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Early-onset myopathy with fatal cardiomyopathy
Other Variants in TTN