rs12722489(C;T)
A slight increase in risk of developing multiple sclerosis
- Magnitude
- 0.0Typical
- Repute
- Bad
- Frequency
- 14%Average of 11 populations
- On SNPedia
- rs12722489(A;G)Minus strand
- Gene
- IL2RA
Frequency
Share of people with C;T in each HapMap population.
- European ancestry (Utah)29%
- Chinese (Denver)23%
- Han Chinese (Beijing)23%
- Japanese (Tokyo)21%
- Tuscan21%
- Gujarati Indian19%
- Mexican ancestry (Los Angeles)9%
- African ancestry (Southwest US)5%
- Maasai (Kenya)3%
- Luhya (Kenya)<1%
- Yoruba (Nigeria)0%
Other genotypes of rs12722489
Related
Source and license
Adapted from rs12722489(A;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.