rs5029939(C;G)
1.67x increased risk of Sjogren's syndrome
- Magnitude
- 0.0Typical
- Repute
- Bad
- Frequency
- 22%Average of 11 populations
- On SNPedia
- rs5029939(C;G)
- Gene
- TNFAIP3
Frequency
Share of people with C;G in each HapMap population.
- Luhya (Kenya)58%
- Yoruba (Nigeria)48%
- Maasai (Kenya)46%
- African ancestry (Southwest US)30%
- Japanese (Tokyo)16%
- Chinese (Denver)12%
- Han Chinese (Beijing)12%
- Tuscan8%
- Gujarati Indian7%
- European ancestry (Utah)5%
- Mexican ancestry (Los Angeles)3%
Other genotypes of rs5029939
Source and license
Adapted from rs5029939(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.