rs9623117

A SNP in the TNRC6B gene on chromosome 22. Its most notable genotype is C;C: 1.1x increased risk for prostate cancer

Gene
TNRC6B
Location
Chr 2240,056,115 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
31%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableBad1.1x increased risk for prostate cancerTypical · 0.026% of people
  2. C;TBad1.1x increased risk for prostate cancerTypical · 0.026% of people
  3. T;TNot ratednormalTypical · 0.048% of people

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 26% C;T 26% T;T 48%
  • European ancestry (Utah)C;C 4% C;T 37% T;T 59%
  • Han Chinese (Beijing)C;C <1% C;T 7% T;T 93%
  • Japanese (Tokyo)C;C 0% C;T 4% T;T 96%
  • Yoruba (Nigeria)C;C 83% C;T 16% T;T <1%
  • African ancestry (Southwest US)C;C 39% C;T 49% T;T 12%
  • Chinese (Denver)C;C 0% C;T 4% T;T 96%
  • Gujarati IndianC;C 9% C;T 55% T;T 37%
  • Luhya (Kenya)C;C 86% C;T 14% T;T <1%
  • Mexican ancestry (Los Angeles)C;C 0% C;T 28% T;T 72%
  • Maasai (Kenya)C;C 56% C;T 40% T;T 5%
  • TuscanC;C 7% C;T 34% T;T 59%

Conditions, medicines and genes

Notes

From SNPedia

Notes

In seven different populations studied, rs9623117(C) was consistently higher in aggressive prostate cancer cases than in controls (p = 5.0 x 10e-7). The odds ratio (OR) of allele C for aggressive prostate cancer was estimated to be 1.18 (CI: 1.11-1.26). This SNP was also associated with increased risk for nonaggressive prostate cancer, with an odds ratio of 1.11 (CI: 1.04 - 1.19, p = 0.004).

Source and license

Adapted from rs9623117 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.