RS2289181 CEP152

Health Risk Chr 15:48797977 snv missense variant

Upload your DNA to see your genotype for this variant.

Population Frequencies

gnomAD ALL

2.3%

1kG AFR

0.7%

1kG ALL

8.7%

1kG AMR

84.6%

1kG EAS

16.2%

1kG EUR

99.5%

1kG SAS

84.6%

Other Variants in CEP152

Ask Dr. Hemsworth about this variant