{{Rsnum
|rsid=1799943
|Gene=BRCA2
|Chromosome=13
|position=32316435
|Orientation=plus
|GMAF=0.2185
|Gene_s=BRCA2
|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 | 2.7 | 34.5 | 62.8
| HCB | 6.6 | 49.3 | 44.1
| JPT | 19.6 | 54.5 | 25.9
| YRI | 0.7 | 10.2 | 89.1
| ASW | 1.8 | 17.5 | 80.7
| CHB | 6.6 | 49.3 | 44.1
| CHD | 12.8 | 41.3 | 45.9
| GIH | 4.0 | 44.6 | 51.5
| LWK | 0.0 | 5.5 | 94.5
| MEX | 1.7 | 36.2 | 62.1
| MKK | 0.0 | 15.4 | 84.6
| TSI | 6.9 | 33.3 | 59.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=22809218
|Title=BRCA2 variants and cardiovascular disease in a multi-ethnic study
|OA=1
}}

{{ClinVar
|ALT=A,C,T
|CAF=0.7815; 0.2185; .
|CHROM=13
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000013.10:g.32890572G>A; NC_000013.10:g.32890572G>C; NC_000013.10:g.32890572G>T
|CLNSIG=1
|COMMON=1
|FwdALT=A,C,T
|FwdREF=G
|GENEINFO=BRCA2:675
|GENE_ID=675
|GENE_NAME=BRCA2
|REF=G
|RSPOS=32890572
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;U5;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;NOV
|VC=SNV
|VP=0x05016840000115051f100104
|WGT=1
|dbSNPBuildID=89
|rsid=1799943
}}

{{PMID Auto
|PMID=12466288
|Title=Haplotype and linkage disequilibrium architecture for human cancer-associated genes.
|OA=1
}}

{{PMID Auto
|PMID=19276285
|Title=Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.
|OA=1
}}

{{PMID Auto
|PMID=19644020
|Title=Genotyping of frequent BRCA1/2 SNPs with unlabeled probes: a supplement to HRMCA mutation scanning, allowing the strong reduction of sequencing burden.
|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}}