rs11650494

A SNP on chromosome 17. Its most notable genotype is A;A: Slightly higher prostate cancer risk

Gene
None listed
Location
Chr 1749,267,824 (GRCh38)
Highest magnitude
1.1Minor
Tested on
23andMe, AncestryDNA
Minor allele frequency
8%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadSlightly higher prostate cancer riskMinor · 1.12% of people
  2. A;GBadSlightly higher prostate cancer riskMinor · 1.115% of people

On SNPedia: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageA;A 2% A;G 15%
  • European ancestry (Utah)A;A 0% A;G 17%
  • Han Chinese (Beijing)A;A 0% A;G 0%
  • Japanese (Tokyo)A;A 0% A;G 0%
  • Yoruba (Nigeria)A;A 6% A;G 44%

Source and license

Adapted from rs11650494 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.