RS886038928 TTN
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What This Variant Does
"CLNSIG=4
Associated Conditions
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiomyopathy
Primary dilated cardiomyopathy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiomyopathy
Primary dilated cardiomyopathy
Other Variants in TTN