{{Rsnum
|rsid=2981575
|Gene=FGFR2
|Chromosome=10
|position=123346116
|Orientation=minus
|GMAF=0.4633
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.7 | 41.6 | 32.7
| HCB | 21.9 | 43.1 | 35.0
| JPT | 13.3 | 46.0 | 40.7
| YRI | 36.7 | 47.6 | 15.6
| ASW | 24.6 | 57.9 | 17.5
| CHB | 21.9 | 43.1 | 35.0
| CHD | 17.4 | 44.0 | 38.5
| GIH | 14.9 | 56.4 | 28.7
| LWK | 34.5 | 51.8 | 13.6
| MEX | 22.4 | 46.6 | 31.0
| MKK | 42.9 | 43.5 | 13.6
| TSI | 20.6 | 44.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=21060860
|Title=Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
|OA=1
}}

{{PMID|19223389|OA=1
}} FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.

{{on chip | Affy GenomeWide 6}}