rs199533(A;A)
Increased risk of developing Parkinson's Disease
- Magnitude
- 2.0Worth knowing
- Repute
- Bad
- Frequency
- 2%Average of 10 populations
- On SNPedia
- rs199533(T;T)Minus strand
- Gene
- NSF
Frequency
Share of people with A;A in each HapMap population.
- Tuscan12%
- Mexican ancestry (Los Angeles)5%
- Gujarati Indian2%
- Maasai (Kenya)1%
- European ancestry (Utah)<1%
- Han Chinese (Beijing)0%
- Japanese (Tokyo)0%
- Yoruba (Nigeria)0%
- African ancestry (Southwest US)0%
- Luhya (Kenya)0%
Other genotypes of rs199533
Notes
From SNPedia
The (T;T) genotype at this position suggests an increased risk of Parkinson's Disease. The homozygote form (T;T) is more common. The other SNP that definitely relates to NSF is rs183211. rs199533 along with rs2736990 and rs393152 were cited in this gwas study regarding the risk of underlying Parkinson’s disease. .
References
Related
Source and license
Adapted from rs199533(T;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.