rs63749932(C;T)

Lynch syndrome; pathogenic mutation

Magnitude
6.0Very important
Repute
Bad
On SNPedia
rs63749932(C;T)
Gene
MSH2

Other genotypes of rs63749932

  1. C;CGoodcommon in clinvarTypical · 0.0
  2. T;TBadLynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)Very important · 6.0

All about rs63749932

Source and license

Adapted from rs63749932(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.