rs16901979
A SNP on chromosome 8. Its most notable genotype is A;A: 1.5x increased risk for prostate cancer
- Gene
- None listed
- Location
- Chr 8127,112,671 (GRCh38)
- Highest magnitude
- 2.9Worth knowing
- Tested on
- 23andMe
- Minor allele frequency
- 18%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBad1.5x increased risk for prostate cancer
- A;CBad1.5x increased risk for prostate cancer
- C;CGoodnormal risk
On SNPedia: (A;A), (A;C), (C;C). 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.
- AverageA;A 8% A;C 33% C;C 60%
- European ancestry (Utah)A;A 0% A;C 6% C;C 94%
- Han Chinese (Beijing)A;A 7% A;C 38% C;C 56%
- Japanese (Tokyo)A;A <1% A;C 34% C;C 66%
- Yoruba (Nigeria)A;A 33% A;C 49% C;C 18%
- African ancestry (Southwest US)A;A 5% A;C 54% C;C 40%
- Chinese (Denver)A;A 6% A;C 43% C;C 51%
- Gujarati IndianA;A 2% A;C 24% C;C 74%
- Luhya (Kenya)A;A 24% A;C 52% C;C 25%
- Mexican ancestry (Los Angeles)A;A 0% A;C 7% C;C 93%
- Maasai (Kenya)A;A 6% A;C 43% C;C 51%
- TuscanA;A 0% A;C 9% C;C 91%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 180 words
rs16901979 is a SNP on chromosome 8q24, associated with increased risk for prostate cancer in several studies. In some studies, the regions have been divided, and this SNP falls in region 2. In a study of over 3,600 Caucasians with prostate cancer, rs16901979 is one of five SNPs used (with family history as a sixth factor) to cumulatively predict overall risk. On their own, the rs16901979(A;A) and (A;C) risk genotypes yield an odds ratio for developing prostate cancer of 1.53 (CI: 1.22-1.92, p=1.8x10e-4) and may account for 3.6% of population attributable risk. cancer related according to this blog Two genetic markers in the 8q24 region of chromosome 8 rs7008482 and rs16901979 have been linked to an increased risk of prostate cancer in African Americans. abstract In follow-up studies looking at disease severity (and not just overall risk), this SNP is reported to account for the risk (from region 2) of advanced prostate cancer. A meta-analysis of 10+ studies comprising over 15,000 prostate cancer patients concluded that the odds ratio for rs16901979(A) allele carriers is 1.74 (CI: 1.72-1.77).
Source and license
Adapted from rs16901979 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.