RS756433029 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
Cardiovascular phenotype
Cardiomyopathy
Left ventricular noncompaction cardiomyopathy
Myopathy
myofibrillar
9
with early respiratory failure
Early-onset myopathy with fatal cardiomyopathy
Hypertrophic cardiomyopathy 9
Tibial muscular dystrophy
Autosomal recessive titinopathy
TTN-related disorder
Other Variants in TTN