rs6280
A SNP in the DRD3 gene on chromosome 3. Its most notable genotype is C;C: better response to olanzapine
- Gene
- DRD3
- Location
- Chr 3114,171,968 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 45%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (C;T), (T;T). 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.
- AverageC;C 31% C;T 41% T;T 28%
- European ancestry (Utah)C;C 15% C;T 41% T;T 44%
- Han Chinese (Beijing)C;C 13% C;T 46% T;T 42%
- Japanese (Tokyo)C;C 6% C;T 48% T;T 46%
- Yoruba (Nigeria)C;C 74% C;T 24% T;T 2%
- African ancestry (Southwest US)C;C 56% C;T 37% T;T 7%
- Chinese (Denver)C;C 13% C;T 36% T;T 51%
- Gujarati IndianC;C 20% C;T 51% T;T 30%
- Luhya (Kenya)C;C 69% C;T 30% T;T <1%
- Mexican ancestry (Los Angeles)C;C 12% C;T 50% T;T 38%
- Maasai (Kenya)C;C 46% C;T 45% T;T 10%
- TuscanC;C 16% C;T 41% T;T 43%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 310 words
rs6280, also known as Ser9Gly, is a SNP in the dopamine receptor D3 DRD3 gene. The rs6280(C) allele encodes a glycine, and the (T) allele encodes a serine (in dbSNP orientation). In a study of 88 patients being treated for schizophrenia with olanzapine, those who were rs6280(C;C) homozygotes had greater positive symptom remission (endpoint rating of minimal or none on all PANSS clinical response positive items, 39.1%), as compared with (C;T) or (T;T) genotypes (13.8%; p = 0.033). Ser9Gly has been implicated in executive function in some studies, but the results are conflicting. * Gly/Gly carriers showed significantly (p = 0.002) poorer performance than Ser/Ser carriers on executive functioning tasks in a somewhat small Caucasian sample (84 patients with first-episode psychosis and 85 controls). * Gly/Ser heterozygotes had 23% more preservative errors on the WCST compared to Ser/Ser homozygotes in a small (216) healthy Han Chinese sample (p = 0.009). Differences between homozygotes were not statistically significant. * No association between WCST scores and Ser9Gly was found in 138 schizophrenic patients. Associated in a family association study and pooled sample of 2,037 with nicotine dependence in Americans of European descent. Preliminary evidence for an association between a dopamine D3 receptor gene variant and obsessive-compulsive personality disorder in patients with major depression. DRD3 polymorphism for an individual with Gly/Gly (C;C) genotype is 2.4 (P = 0.017) times more likely to be diagnosed with OCPD. Male gender was also found to be a significant predictor of OCPD diagnosis (OR = 2.82, P = 0.001). DRD3 may contribute to the development of OCPD. This association was tested using two independent groups of individuals with a history of depression, from a clinical sample (n = 149) and a family study (n = 213).
Source and license
Adapted from rs6280 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.