{{Rsnum
|rsid=4973768
|Gene=SLC4A7
|Chromosome=3
|position=27374522
|Orientation=plus
|GMAF=0.3669
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC4A7
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.9 | 59.8 | 14.3
| HCB | 67.2 | 29.2 | 3.6
| JPT | 69.0 | 27.4 | 3.5
| YRI | 50.3 | 40.7 | 9.0
| ASW | 49.1 | 38.6 | 12.3
| CHB | 67.2 | 29.2 | 3.6
| CHD | 68.8 | 27.5 | 3.7
| GIH | 33.7 | 45.5 | 20.8
| LWK | 58.7 | 33.0 | 8.3
| MEX | 8.6 | 51.7 | 39.7
| MKK | 38.1 | 45.8 | 16.1
| TSI | 21.6 | 56.9 | 21.6
| 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=6E-7
|OR=1.16
|ORtxt=[1.10-1.24]
|OA=1
}}

{{PMID Auto
|PMID=20699374
|Title=Evaluation of Breast Cancer Susceptibility Loci in Chinese Women
|OA=1
}}
{{PMID Auto
|PMID=21118973
|Title=Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
|OA=1
}}

{{omim
|id=114480
|rsnum=4973768
}}

{{PMID Auto GWAS
|PMID=21263130
|Trait=None
|Title=Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study
|RiskAllele=C
|Pval=2E-8
|OR=1.1400
|ORtxt=[1.09-1.19]
}}

{{PMID Auto
|PMID=21415360
|Title=Common genetic variants associated with breast cancer in Korean women and differential susceptibility according to intrinsic subtype
}}

{{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=21791674
|Title=Interactions Between Genetic Variants and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium
|OA=1
}}

{{PMID Auto
|PMID=22287734
|Title=Evaluation of Breast Cancer Susceptibility Loci on 2q35, 3p24, 17q23 and FGFR2 Genes in Taiwanese Women with Breast Cancer
}}

{{PMID Auto
|PMID=19330027
|Title=Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
|OA=1
}}

{{PMID Auto
|PMID=19639606
|Title=Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
|OA=1
}}

{{PMID Auto
|PMID=20146796
|Title=Familial relative risks for breast cancer by pathological subtype: a population-based cohort study.
|OA=1
}}

{{PMID Auto
|PMID=21596841
|Title=Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium.
|OA=1
}}

{{PMID Auto
|PMID=22160591
|Title=A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population.
}}

{{PMID Auto
|PMID=22532573
|Title=The role of genetic breast cancer susceptibility variants as prognostic factors.
|OA=1
}}

{{PMID Auto
|PMID=23117855
|Title=The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case-control study and a meta-analysis
}}

{{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-30
  |OR=1.10
  |ORtxt=[1.08-1.12]
  |OA=1
}}

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