rs11246226
A SNP in the DRD4 gene on chromosome 11. Its most notable genotype is A;C: decreased risk of schizophrenia in limited study
- Gene
- DRD4
- Location
- Chr 11641,191 (GRCh38)
- Highest magnitude
- 1.2Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;ABadincreased risk of schizophrenia in limited study
- A;CMost notableGooddecreased risk of schizophrenia in limited study
- C;CGooddecreased risk of schizophrenia in limited study
On SNPedia: (A;A), (A;C), (C;C). 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 29% A;C 46% C;C 24%
- European ancestry (Utah)A;A 23% A;C 56% C;C 21%
- Han Chinese (Beijing)A;A 61% A;C 35% C;C 4%
- Japanese (Tokyo)A;A 55% A;C 36% C;C 9%
- Yoruba (Nigeria)A;A 14% A;C 51% C;C 34%
- African ancestry (Southwest US)A;A 14% A;C 61% C;C 25%
- Chinese (Denver)A;A 57% A;C 36% C;C 7%
- Gujarati IndianA;A 32% A;C 46% C;C 22%
- Luhya (Kenya)A;A 7% A;C 40% C;C 54%
- Mexican ancestry (Los Angeles)A;A 18% A;C 56% C;C 26%
- Maasai (Kenya)A;A 18% A;C 46% C;C 37%
- TuscanA;A 25% A;C 47% C;C 28%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
Associated with schizophrenia in a study of Croatians. Due to the limited number and diversity of the studied population, more study is needed to confirm any link. The C allele was associated with an decreased risk of schizophrenia.
Source and license
Adapted from rs11246226 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.