RS118161093 TTN

Health Risk Chr 2:178776123 snv missense variant
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Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2J
Dilated cardiomyopathy 1G
Cardiovascular phenotype
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
0.2%
1kG EUR
100%
1kG SAS
100%
Other Variants in TTN
rs28933405 rs2154172276 rs267607155 rs281864927 rs267607156 rs281864928 rs267607158 rs147879266 rs138060032 rs587776772
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