rs167771
A SNP in the DRD3 gene on chromosome 3. Its most notable genotype is G;G.
- Gene
- DRD3
- Location
- Chr 3114,157,428 (GRCh38)
- Highest magnitude
- 1.1Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 35%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (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 39% G;G 27%
- European ancestry (Utah)A;A 67% G;G 4%
- Han Chinese (Beijing)A;A 63% G;G <1%
- Japanese (Tokyo)A;A 72% G;G 4%
- Yoruba (Nigeria)A;A 2% G;G 76%
- African ancestry (Southwest US)A;A 12% G;G 39%
- Chinese (Denver)A;A 66% G;G 4%
- Gujarati IndianA;A 33% G;G 16%
- Luhya (Kenya)A;A 0% G;G 86%
- Mexican ancestry (Los Angeles)A;A 45% G;G 7%
- Maasai (Kenya)A;A 9% G;G 55%
- TuscanA;A 61% G;G 5%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs167771 was significantly associated with autism spectrum disorder in a study of 144 patients. G allele associated with increased extra-pyramidal symptom risk as a result of risperidone treatment in a study of 321 psychiatric inpatients (81 presenting with EPS and 189 without)
A;A
Possibly more "Insistence on Sameness" on ADI-R test.ncbi.nlm.nih.gov Possibly increased FTND nicotine dependence.ncbi.nlm.nih.gov
G;G
Increased extra-pyramidal symptom risk as a result of risperidone treatment in a study of 321 psychiatric inpatients. Possibly less "Insistence on Sameness" in ADI-R test.
Source and license
Adapted from rs167771 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.