{{Rsnum
|rsid=12559632
|Gene=PHEX
|Chromosome=X
|position=22142875
|Orientation=plus
|GMAF=0.3089
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PHEX
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.2 | 22.1 | 63.7
| HCB | 35.8 | 28.5 | 35.8
| JPT | 30.1 | 22.1 | 47.8
| YRI | 18.4 | 13.6 | 68.0
| ASW | 19.3 | 26.3 | 54.4
| CHB | 35.8 | 28.5 | 35.8
| CHD | 39.4 | 22.0 | 38.5
| GIH | 15.8 | 14.9 | 69.3
| LWK | 15.5 | 19.1 | 65.5
| MEX | 32.8 | 17.2 | 50.0
| MKK | 16.0 | 24.4 | 59.6
| TSI | 22.5 | 13.7 | 63.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21326311
|Trait=None
|Title=Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
|RiskAllele=A
|Pval=0.000003
|OR=1.1600
|ORtxt=[0.69-1.63] unit decrease
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}