RS72646846 TTN

Health Risk Chr 2:178589849
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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
Cardiomyopathy
6 conditions
Cardiovascular phenotype
Primary familial dilated cardiomyopathy
Autosomal recessive titinopathy
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiomyopathy
6 conditions
Cardiovascular phenotype
Primary familial dilated cardiomyopathy
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
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