rs828907
A SNP in the XRCC5 gene on chromosome 2. Its most notable genotype is G;T: Slightly increased risk of bladder cancer and 2x risk of developing bladder cancer in smokers
- Gene
- XRCC5
- Location
- Chr 2216,108,009 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 30%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodNormal risk of developing bladder cancer
- G;TMost notableBadSlightly increased risk of bladder cancer and 2x risk of developing bladder cancer in smokers
- T;TBadIncreased risk of bladder cancer and 2x risk of developing bladder cancer in smokers
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 11 HapMap populations.
- AverageG;G 54% G;T 35% T;T 11%
- European ancestry (Utah)G;G 28% G;T 48% T;T 24%
- Han Chinese (Beijing)G;G 64% G;T 32% T;T 4%
- Japanese (Tokyo)G;G 62% G;T 30% T;T 8%
- Yoruba (Nigeria)G;G 67% G;T 31% T;T 2%
- African ancestry (Southwest US)G;G 65% G;T 32% T;T 4%
- Chinese (Denver)G;G 67% G;T 29% T;T 4%
- Gujarati IndianG;G 19% G;T 47% T;T 35%
- Luhya (Kenya)G;G 75% G;T 22% T;T 3%
- Mexican ancestry (Los Angeles)G;G 59% G;T 22% T;T 19%
- Maasai (Kenya)G;G 55% G;T 41% T;T 4%
- TuscanG;G 37% G;T 48% T;T 15%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs828907, also known as G-1401T, is a SNP in the Ku80 gene. A study of 288 Chinese patients with bladder cancer and 288 age- and gender-matched healthy controls found that the rs828907(T) allele conferred a significant (p=0.0055) increased risk of bladder cancer. In association with smoking, the (G;T) and (T;T) genotypes conferred a 2x risk (CI:1.232-3.419) for bladder cancer. correlated with oral cancer susceptibility
Source and license
Adapted from rs828907 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.