RS371678190 TTN
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What This Variant Does
"CLNSIG=5
Associated Conditions
Primary dilated cardiomyopathy
Primary familial dilated cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2J
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiomyopathy
Cardiovascular phenotype
Primary dilated cardiomyopathy
Primary familial dilated cardiomyopathy
Cardiomyopathy
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Other Variants in TTN