RS368327166 TTN

Health Risk Chr 2:178679958 delins inframe insertion
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Associated Conditions
Ventricular fibrillation
paroxysmal familial
type 1
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Cardiomyopathy
Brugada syndrome
Primary dilated cardiomyopathy
Ventricular fibrillation
paroxysmal familial
type 1
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Population Frequencies
gnomAD ALL
98.3%
1kG AFR
99.9%
1kG ALL
0.5%
1kG AMR
99.4%
1kG EAS
100%
1kG EUR
98.5%
1kG SAS
99.7%
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
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