rs12476364(G;T)

Lynch syndrome

Magnitude
6.0Very important
Repute
Bad
Frequency
0%Average of 4 populations
On SNPedia
rs12476364(G;T)
Gene
MSH2

Frequency

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

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs12476364

  1. A;GMost notableBadLynch syndrome, pathogenic mutationVery important · 6.00% of people
  2. C;GBadLynch syndrome, pathogenic mutationVery important · 6.00% of people
  3. G;GGoodcommon in clinvarTypical · 0.0100% of people

All about rs12476364

Source and license

Adapted from rs12476364(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.