{{Rsnum
|rsid=614367
|Chromosome=11
|position=69513996
|Orientation=plus
|GMAF=0.09963
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 68.5 | 26.1 | 5.4
| HCB | 98.5 | 1.5 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 76.2 | 22.4 | 1.4
| ASW | 84.2 | 15.8 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 65.0 | 33.0 | 2.0
| LWK | 73.4 | 22.0 | 4.6
| MEX | 89.7 | 10.3 | 0.0
| MKK | 60.9 | 37.2 | 1.9
| TSI | 73.3 | 25.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20453838
|Trait=Breast cancer
|Title=Genome-wide association study identifies five new breast cancer susceptibility loci
|RiskAllele=T
|Pval=3E-15
|OR=1.15
|ORtxt=[1.10-1.20]
|OA=1
}}

{{PMID Auto
|PMID=21445572
|Title=Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies
}}

{{PMID Auto
|PMID=22348646
|Title=Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
|OA=1
}}

{{PMID Auto
|PMID=22461340
|Title=11q13 is a susceptibility locus for hormone receptor positive breast cancer
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23535729
  |Trait=Breast cancer
  |Title=Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
  |RiskAllele=T
  |Pval=2E-63
  |OR=1.21
  |ORtxt=[1.18-1.24]
  |OA=1
}}

{{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}}