{{Rsnum
|rsid=11571833
|Gene=BRCA2
|Chromosome=13
|position=32398489
|Orientation=plus
|ReferenceAllele=A
|GMAF=0.00551
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=BRCA2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 98.5 | 1.5 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

This SNP, a variant in the [[BRCA2]] gene, is 1 of 25 SNPs reported to represent independently minor, but cumulatively significant, increased risk for [[breast cancer]]. {{PMID|17341484}}

For details of all 25 SNPs in this group, along with the two methods used to calculate overall risk estimates for [[breast cancer]], refer to the SNPedia [[breast cancer]] entry.

For this particular SNP, the risk (minor) allele is (T).
{{ neighbor
| rsid = 1801426
| distance = 258
}}

{{ClinVar
|rsid=11571833
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=32972626
|CHROM=13
|GMAF=0.0055
|dbSNPBuildID=120
|SSR=0
|SAO=0
|VP=0x050168000000040517120101
|GENEINFO=BRCA2:675
|GENE_NAME=BRCA2
|GENE_ID=675
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.32972626A>T
|CLNSIG=2
|Tags=PM;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;MTP
|CAF=0.9945; 0.00551
|CLNACC=RCV000031849.3; RCV000034474.1; RCV000045926.2
|CLNDBN=Breast-ovarian cancer, familial 2; not provided; Familial cancer of breast
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1247:C2675520:612555:145; NBK1247:C0346153:114480:254843006
|COMMON=1
|Disease=Breast-ovarian cancer; not provided; Familial cancer of breast
}}

{{PMID Auto
|PMID=18974781
|Title=Cataloging coding sequence variations in human genome databases.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23535733
  |Trait=Breast cancer
  |Title=Genome-wide association studies identify four ER negative-specific breast cancer risk loci.
  |RiskAllele=T
  |Pval=6E-6
  |OR=1.52
  |ORtxt=[1.31-1.77]
  |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=5E-8
  |OR=1.26
  |ORtxt=[1.14-1.39]
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}