{{Rsnum
|rsid=17101921
|Chromosome=10
|position=123153295
|Orientation=plus
|GMAF=0.07805
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 2.7 | 97.3
| HCB | 5.1 | 21.2 | 73.7
| JPT | 3.5 | 38.9 | 57.5
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 5.1 | 21.2 | 73.7
| CHD | 0.0 | 31.2 | 68.8
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 3.4 | 24.1 | 72.4
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 6.9 | 93.1
| HapMapRevision=28
}}

A very large (ultimately over 7,000 cases spanning multiple European Caucasians) study concluded that [[rs17101921]] showed evidence for association with [[schizophrenia]], with an odds ratio of 1.17 (CI: 1.06-1.29, p=0.0009).{{PMID|18813210|OA=1
}}

{{PMID Auto
|PMID=22404656
|Title=FGFR2 is associated with bipolar disorder: A large-scale case-control study of three psychiatric disorders in the Chinese Han population
}}

{{PMID Auto
|PMID=19721717
|Title=Apoptotic engulfment pathway and schizophrenia.
|OA=1
}}

{{PMID Auto
|PMID=19911060
|Title=Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}