rs12777823(G;G)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
Frequency
59%Average of 11 populations
On SNPedia
rs12777823(G;G)
Gene
LOC100130970

Frequency

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

  • Tuscan80%
  • Mexican ancestry (Los Angeles)74%
  • European ancestry (Utah)74%
  • African ancestry (Southwest US)67%
  • Maasai (Kenya)60%
  • Chinese (Denver)54%
  • Luhya (Kenya)53%
  • Gujarati Indian53%
  • Yoruba (Nigeria)52%
  • Japanese (Tokyo)46%
  • Han Chinese (Beijing)43%

Other genotypes of rs12777823

  1. A;AMost notableBadAvoid Plavix, higher risk for adverse cardiovascular events. CYP2C19 poor metabolizer.Important · 3.56% of people
  2. A;GBadAvoid Plavix, higher risk for adverse cardiovascular events.Worth knowing · 2.534% of people

All about rs12777823

Source and license

Adapted from rs12777823(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.