rs11214613
A SNP in the DRD2 gene on chromosome 11. Its most notable genotype is G;G: common in complete genomics
- Gene
- DRD2
- Location
- Chr 11113,464,537 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
- Minor allele frequency
- 23%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 48%
- European ancestry (Utah)G;G 73%
- Han Chinese (Beijing)G;G 57%
- Japanese (Tokyo)G;G 54%
- Yoruba (Nigeria)G;G 9%
Related
Other DRD2 SNPs
- rs6277A;Anormal schizophrenia risk, learns NoGo fasterWorth knowing
- rs1076560A;Ainfluences working memoryWorth knowing
- rs1799732-;-less favorable clinical outcome when on antipsychoticsWorth knowing
- rs4648317A;Aprone to higher nicotine dependence, more impulsive/sensation seekingMinor
- rs6275A;Acommon in clinvarTypical
- rs1799978T;Tcommon in clinvarTypical
- rs1800496G;Gcommon in complete genomicsTypical
- rs1801028G;Gnormal riskTypical
Source and license
Adapted from rs11214613 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.