RS397517628 TTN

Health Risk Chr 2:178597955
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What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Autosomal recessive titinopathy
Primary dilated cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Autosomal recessive titinopathy
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
Ask Dr. Hemsworth about this variant