rs1050828(C;C)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
Frequency
90%Average of 8 populations
On SNPedia
rs1050828(G;G)Minus strand
Gene
G6PD

Frequency

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

  • European ancestry (Utah)100%
  • Han Chinese (Beijing)100%
  • Japanese (Tokyo)100%
  • Mexican ancestry (Los Angeles)98%
  • Maasai (Kenya)98%
  • African ancestry (Southwest US)79%
  • Luhya (Kenya)76%
  • Yoruba (Nigeria)69%

Other genotypes of rs1050828

  1. -;CGoodNo summary available.Typical · 0.00% of people
  2. T;TMost notableBadG6PD deficiency; Hb1Ac value may need adjusting for diabetes diagnosisVery important · 4.03% of people
  3. C;TBadG6PD deficiency carrier; Hb1Ac value may need adjusting for diabetes diagnosisImportant · 3.07% of people
  4. -;CGoodNo summary available.Typical · 0.00% of people

All about rs1050828

Notes

From SNPedia

The rs1050828 G allele is located within the G6PD gene and is associated with 'normal' levels of glucose-6-phosphate dehydrogenase enzyme production.

Source and license

Adapted from rs1050828(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.