RS115958467 PIGL

Health Risk Chr 17:16299975 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
gnomAD ALL
0.6%
1kG AFR
100%
1kG ALL
0.2%
1kG AMR
0.9%
1kG EAS
100%
1kG EUR
99.5%
1kG SAS
100%
Other Variants in PIGL
Ask Dr. Hemsworth about this variant