rs9567552
A SNP in the BRCA2 gene on chromosome 13. Its most notable genotype is G;G: common/normal
- Gene
- BRCA2
- Location
- Chr 1332,316,090 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 22%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 53% G;T 40% T;T 7%
- European ancestry (Utah)G;G 52% G;T 42% T;T 6%
- Han Chinese (Beijing)G;G 60% G;T 33% T;T 7%
- Japanese (Tokyo)G;G 29% G;T 58% T;T 13%
- Yoruba (Nigeria)G;G 70% G;T 29% T;T 2%
Related
Conditions, medicines and genes
Other BRCA2 SNPs
- i5009091D;Ilikely to be BRCA2 variant pathogenic for breast cancerVery important
- rs4987049A;CBRCA2 variant considered pathogenic for breast cancerVery important
- rs11571658-;TTBRCA2 variant considered pathogenic for breast cancerVery important
- rs28897743A;Gconsidered a causal BRCA2 breast cancer mutationVery important
- rs28897746C;TBRCA2 variant considered pathogenic for breast cancerVery important
- rs28897756A;ABRCA2, breast cancer mutationVery important
- rs41293477G;TBRCA2 variant considered pathogenic for breast cancerVery important
- rs41293489C;GBRCA2 variant considered pathogenic for breast cancerVery important
Notes
From SNPedia
Notes
Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk. LD2SNPing: linkage disequilibrium plotter and RFLP enzyme mining for tag SNPs.
T;T
rs9567552, also known as c.-39-332G>T, is a variant in the BRCA2 gene considered benign by multiple ClinVar submitters.
Source and license
Adapted from rs9567552 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.