RS794729324 TTN
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Primary familial dilated cardiomyopathy
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Primary familial dilated cardiomyopathy
Other Variants in TTN