rs1801157
A SNP in the CXCL12 gene on chromosome 10. Its most notable genotype is T;T: 1.4x higher risk for breast cancer
- Gene
- CXCL12
- Location
- Chr 1044,372,809 (GRCh38)
- Highest magnitude
- 1.4Minor
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 21%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableBad1.4x higher risk for breast cancer
- C;TBad1.4x higher risk for breast cancer
- C;CNot ratedNo summary available.
SNPedia records rs1801157 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 5% C;T 27% C;C 68%
- European ancestry (Utah)T;T 4% C;T 35% C;C 62%
- Han Chinese (Beijing)T;T 10% C;T 31% C;C 59%
- Japanese (Tokyo)T;T 9% C;T 40% C;C 51%
- Yoruba (Nigeria)T;T 0% C;T 4% C;C 96%
- African ancestry (Southwest US)T;T 0% C;T 16% C;C 84%
- Chinese (Denver)T;T 9% C;T 39% C;C 51%
- Gujarati IndianT;T 10% C;T 46% C;C 45%
- Luhya (Kenya)T;T 0% C;T 13% C;C 87%
- Mexican ancestry (Los Angeles)T;T 2% C;T 29% C;C 69%
- Maasai (Kenya)T;T 1% C;T 13% C;C 86%
- TuscanT;T 9% C;T 35% C;C 56%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs1801157, also known as G801A, is a SNP in the chemokine (C-X-C motif) ligand 12 CXCL12 gene. rs1801157(A) was associated with protection against infection (OR=0.63, P=0.01). In the MACS cohort, rs1801157 was associated with AIDS-87 (RH=0.31, P=0.02) and with death (RH=0.18, P=0.02). HIV-1/AIDS A 2011 meta-analysis (comprising 5 studies totaling 1,058 cases) found that the rs1801157(A) allele was associated with higher risk for breast cancer, with an odds ratio of 1.44 (CI: 1.2 - 1.7; under a dominant model).
Source and license
Adapted from rs1801157 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.