{{Rsnum
|rsid=10760502
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FPGS
|position=127802988
|Gene_s=FPGS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 9.3 | 90.7
| YRI | 0.0 | 0.0 | 0.0
| ASW | 3.6 | 26.8 | 69.6
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.9 | 13.6 | 85.5
| MEX | 17.5 | 45.6 | 36.8
| MKK | 0.0 | 0.0 | 0.0
| TSI | 20.2 | 50.5 | 29.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24762994
|Title=[Correlation Analysis of FPGS rs10760502G&gt;A Polymorphism with Prognosis and MTX-related Toxicity in Pediatric B-cell Acute Lymphoblastic Leukemia]
}}

{{on chip | Illumina Human 1M}}