rs498872(A;G)

1.2x higher risk for glioma development

Magnitude
1.2Minor
Repute
Bad
Frequency
32%Average of 11 populations
On SNPedia
rs498872(C;T)Minus strand
Gene
PHLDB1

Frequency

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

  • Gujarati Indian52%
  • Chinese (Denver)51%
  • Tuscan43%
  • European ancestry (Utah)40%
  • Han Chinese (Beijing)34%
  • Mexican ancestry (Los Angeles)32%
  • Japanese (Tokyo)31%
  • African ancestry (Southwest US)27%
  • Luhya (Kenya)18%
  • Yoruba (Nigeria)13%
  • Maasai (Kenya)12%

Other genotypes of rs498872

  1. G;GNot ratedNo summary available.Typical · 0.062% of people
  2. A;AMost notableBad1.4x higher risk for glioma developmentMinor · 1.46% of people

All about rs498872

Source and license

Adapted from rs498872(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.