rs1223271
A SNP in the TASP1 gene on chromosome 20. Its most notable genotype is A;A: Increased risk of developing Parkinson's Disease
- Gene
- TASP1
- Location
- Chr 2013,316,265 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadIncreased risk of developing Parkinson's Disease
- A;GBadSlightly increased risk of developing Parkinson's Disease
- G;GGoodNormal risk of developing Parkinson's Disease
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 7% A;G 24% G;G 69%
- European ancestry (Utah)A;A 3% A;G 17% G;G 80%
- Han Chinese (Beijing)A;A 21% A;G 49% G;G 31%
- Japanese (Tokyo)A;A 12% A;G 49% G;G 39%
- Yoruba (Nigeria)A;A 0% A;G 0% G;G 100%
- African ancestry (Southwest US)A;A 0% A;G 5% G;G 95%
- Chinese (Denver)A;A 19% A;G 41% G;G 39%
- Gujarati IndianA;A 8% A;G 42% G;G 51%
- Luhya (Kenya)A;A 0% A;G 3% G;G 97%
- Mexican ancestry (Los Angeles)A;A 9% A;G 28% G;G 64%
- Maasai (Kenya)A;A 0% A;G 7% G;G 93%
- TuscanA;A 2% A;G 29% G;G 69%
Source and license
Adapted from rs1223271 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.