RS139063843 PHGDH

Health Risk Chr 1:119735332 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
99.9%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.2%
1kG SAS
100%
Other Variants in PHGDH
Ask Dr. Hemsworth about this variant