RS1064793560 TTN
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
6 conditions
Hypertrophic cardiomyopathy 9
Tibial muscular dystrophy
Myopathy
myofibrillar
9
with early respiratory failure
Early-onset myopathy with fatal cardiomyopathy
TTN-related disorder
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Other Variants in TTN