{{Rsnum
|rsid=12652447
|Gene=FBXL7
|Chromosome=5
|position=15674526
|Orientation=plus
|GMAF=0.4761
|Gene_s=FBXL7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.0 | 50.4 | 26.5
| HCB | 35.8 | 42.3 | 21.9
| JPT | 40.2 | 39.3 | 20.5
| YRI | 34.7 | 51.7 | 13.6
| ASW | 40.4 | 50.9 | 8.8
| CHB | 35.8 | 42.3 | 21.9
| CHD | 35.8 | 50.9 | 13.2
| GIH | 20.8 | 51.5 | 27.7
| LWK | 50.0 | 40.0 | 10.0
| MEX | 19.0 | 37.9 | 43.1
| MKK | 35.9 | 49.4 | 14.7
| TSI | 19.8 | 43.6 | 36.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=24528085
|Title=Breast Cancer Association Studies in a Han Chinese Population using 10 European-ancestry-associated Breast Cancer Susceptibility SNPs
}}

{{PMID Auto
|PMID=20418484
|Title=Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}