rs1800496
A SNP in the DRD2 gene on chromosome 11. Its most notable genotype is G;G: common in complete genomics
- Gene
- DRD2
- Location
- Chr 11113,412,766 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- <1%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1800496 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 3 HapMap populations.
- AverageG;G 100%
- Han Chinese (Beijing)G;G 100%
- Japanese (Tokyo)G;G 100%
- Yoruba (Nigeria)G;G 100%
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
- rs1801028G;Gnormal riskTypical
- rs11214606C;Ccommon on affy axiom dataTypical
Notes
From SNPedia
Notes
origins associated with an independent aspect of decision making in a learning paradigm
Source and license
Adapted from rs1800496 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.