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rs1800496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1800496(C;T)
Make rs1800496(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position113412766
GeneDRD2
is asnp
is mentioned by
dbSNPrs1800496
ebirs1800496
HLIrs1800496
Exacrs1800496
Varsomers1800496
Maprs1800496
PheGenIrs1800496
hapmaprs1800496
1000 genomesrs1800496
hgdprs1800496
ensemblrs1800496
gopubmedrs1800496
geneviewrs1800496
scholarrs1800496
googlers1800496
pharmgkbrs1800496
gwascentralrs1800496
openSNPrs1800496
23andMers1800496
23andMe allrs1800496
SNP Nexus

SNPshotrs1800496
SNPdbers1800496
MSV3drs1800496
GWAS Ctlgrs1800496
GMAF0.001377
Max Magnitude0
? (C;C) (C;T) (T;T) 28
origins associated with an independent aspect of decision making in a learning paradigm
Neighborrs1801028
Distance4
Neighborrs1076560
Distance200


[PMID 19512960] Genetic diagnostics of functional variants of the human dopamine D2 receptor gene


[PMID 18332877OA-icon.png] Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.