rs2697962(C;T)
Slightly increased risk of developing Parkinson's Disease
- Magnitude
- 1.5Minor
- Repute
- Bad
- Frequency
- 29%Average of 11 populations
- On SNPedia
- rs2697962(A;G)Minus strand
- Gene
- PRDM2
Frequency
Share of people with C;T in each HapMap population.
- Gujarati Indian53%
- Japanese (Tokyo)40%
- Mexican ancestry (Los Angeles)33%
- Chinese (Denver)31%
- Han Chinese (Beijing)28%
- Maasai (Kenya)27%
- Tuscan26%
- European ancestry (Utah)25%
- Luhya (Kenya)22%
- Yoruba (Nigeria)20%
- African ancestry (Southwest US)18%
Other genotypes of rs2697962
Source and license
Adapted from rs2697962(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.