rs63750875(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs63750875(G;G)
Gene
MSH2

Other genotypes of rs63750875

  1. C;CMost notableBadLynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)Very important · 7.0
  2. C;GBadLynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)Very important · 6.0

All about rs63750875

Source and license

Adapted from rs63750875(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.