RS138427178 PDE11A

Health Risk Chr 2:177816910 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
100%
1kG ALL
99.9%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.2%
1kG SAS
99.8%
Other Variants in PDE11A
Ask Dr. Hemsworth about this variant