rs13149290
A SNP in the ZNF827 gene on chromosome 4. Its most notable genotype is C;C: Slightly increased risk of developing prostate cancer
- Gene
- ZNF827
- Location
- Chr 4145,829,814 (GRCh38)
- Highest magnitude
- 1.5Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 42%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableBadSlightly increased risk of developing prostate cancer
- C;TBadSlightly increased risk of developing prostate cancer
- T;TGoodNormal risk of developing prostate cancer
On SNPedia: (C;C), (C;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.
- AverageC;C 37% C;T 35% T;T 28%
- European ancestry (Utah)C;C 63% C;T 37% T;T 0%
- Han Chinese (Beijing)C;C 4% C;T 25% T;T 71%
- Japanese (Tokyo)C;C 6% C;T 24% T;T 70%
- Yoruba (Nigeria)C;C 63% C;T 29% T;T 8%
- African ancestry (Southwest US)C;C 63% C;T 30% T;T 7%
- Chinese (Denver)C;C 3% C;T 24% T;T 73%
- Gujarati IndianC;C 28% C;T 48% T;T 25%
- Luhya (Kenya)C;C 53% C;T 42% T;T 5%
- Mexican ancestry (Los Angeles)C;C 17% C;T 48% T;T 35%
- Maasai (Kenya)C;C 51% C;T 43% T;T 6%
- TuscanC;C 54% C;T 38% T;T 8%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs13149290 is one of seven SNPs found in a combined study of over 1,000 patients to be associated with increased risk for prostate cancer. The risk allele for this SNP is (C); and while the odds ratio was not specifically reported, the probability of false significance (not permuted though) was given as p=2.5 x 10e-5, using a dominant model of risk.
Source and license
Adapted from rs13149290 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.