rs2020912(C;T)

Unclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)

Magnitude
2.5Worth knowing
Repute
Bad
Frequency
2%Average of 10 populations
On SNPedia
rs2020912(C;T)
Gene
MSH6

Frequency

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

  • Tuscan6%
  • African ancestry (Southwest US)4%
  • Yoruba (Nigeria)2%
  • Gujarati Indian2%
  • European ancestry (Utah)2%
  • Han Chinese (Beijing)2%
  • Japanese (Tokyo)<1%
  • Chinese (Denver)<1%
  • Luhya (Kenya)<1%
  • Maasai (Kenya)<1%

Other genotypes of rs2020912

  1. T;TGoodcommon in clinvarTypical · 0.098% of people

All about rs2020912

Notes

From SNPedia

This variant is probably benign, but there is a possibility it is associated with hereditary nonpolyposis colorectal cancer type-5 (HNPCC5).

Source and license

Adapted from rs2020912(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.