rs1566734(C;C)

Somatic mutation found once in a colon cancer

Magnitude
1.0Minor
Repute
Bad
Frequency
4%Average of 11 populations
On SNPedia
rs1566734(G;G)Minus strand
Gene
PTPRJ

Frequency

Share of people with C;C in each HapMap population.

  • Gujarati Indian7%
  • Tuscan7%
  • Han Chinese (Beijing)7%
  • Chinese (Denver)6%
  • Japanese (Tokyo)4%
  • African ancestry (Southwest US)4%
  • European ancestry (Utah)2%
  • Mexican ancestry (Los Angeles)2%
  • Maasai (Kenya)1%
  • Yoruba (Nigeria)<1%
  • Luhya (Kenya)0%

Other genotypes of rs1566734

  1. T;TNot ratedNo summary available.Typical · 0.00% of people
  2. A;CBadSomatic mutation, cancer associatedTypical · 0.527% of people
  3. A;AGoodcommon in clinvarTypical · 0.069% of people

All about rs1566734

Notes

From SNPedia

this is *not* reported to be a germline mutation of the type reported to increase one's colon cancer risk

Source and license

Adapted from rs1566734(G;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.