RS117788141 CARS2

Health Risk Chr 13:110705551 snv missense variant
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Associated Conditions
Combined oxidative phosphorylation defect type 27
Combined oxidative phosphorylation defect type 27
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.1%
1kG SAS
100%
Other Variants in CARS2
rs1887501594 rs1412483498 rs372734645 rs758217572 rs201577762 rs1232251739 rs138372705 rs779385700 rs749680674 rs374751888
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