{{Rsnum
|rsid=766173
|Gene=BRCA2
|Chromosome=13
|position=32332343
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=C
|GMAF=0.05831
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=BRCA2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 6.2 | 93.8
| HCB | 0.0 | 27.6 | 72.4
| JPT | 0.0 | 15.2 | 84.8
| YRI | 0.0 | 2.0 | 98.0
| ASW | 0.0 | 3.6 | 96.4
| CHB | 0.0 | 27.6 | 72.4
| CHD | 0.9 | 18.3 | 80.7
| GIH | 2.0 | 28.0 | 70.0
| LWK | 0.0 | 3.7 | 96.3
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.0 | 3.9 | 96.1
| TSI | 2.9 | 6.9 | 90.2
| 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 (G).
{{ neighbor
| rsid = 144848
| distance = 249
}}

{{ClinVar
|rsid=766173
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=32906480
|CHROM=13
|GMAF=0.0582
|dbSNPBuildID=86
|SSR=0
|SAO=0
|VP=0x050168000000150517100100
|GENEINFO=BRCA2:675
|GENE_NAME=BRCA2
|GENE_ID=675
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000013.10:g.32906480A>C; NC_000013.10:g.32906480A>G
|CLNSIG=2
|CLNCUI=
|CLNACC=
RCV000034465.1; RCV000031759.2; RCV000045592.2
|Tags=RV;PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD
|CAF=0.9417; 0.05831; .
|CLNDBN=not provided; Breast-ovarian cancer, familial 2; 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=not provided; Breast-ovarian cancer; Familial cancer of breast
}}

{{PMID Auto
|PMID=16857995
|Title=Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes.
|OA=1
}}

{{GET Evidence
|gene=BRCA2
|aa_change=Asn289His
|aa_change_short=N289H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs766173
|overall_frequency_n=312
|overall_frequency_d=10746
|overall_frequency=0.0290341
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=4
|n_web_uneval=10
}}

{{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}}