RS752948913 TTN
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Tibial muscular dystrophy
Hypertrophic cardiomyopathy 9
Early-onset myopathy with fatal cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Tibial muscular dystrophy
Hypertrophic cardiomyopathy 9
Early-onset myopathy with fatal cardiomyopathy
Other Variants in TTN