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rs167771

From SNPedia

Individuals carrying the AA variant of the rs167771 SNP scored significantly higher on the IS-factor (resp U = 590, p < .01), indicating more rigid behavior than individuals carrying one or two copies of the minor G-allele.
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1
(G;G) 1.1
Make rs167771(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position114157428
GeneDRD3
is asnp
is mentioned by
dbSNPrs167771
dbSNP (classic)rs167771
ClinGenrs167771
ebirs167771
HLIrs167771
Exacrs167771
Gnomadrs167771
Varsomers167771
LitVarrs167771
Maprs167771
PheGenIrs167771
Biobankrs167771
1000 genomesrs167771
hgdprs167771
ensemblrs167771
geneviewrs167771
scholarrs167771
googlers167771
pharmgkbrs167771
gwascentralrs167771
openSNPrs167771
23andMers167771
SNPshotrs167771
SNPdbers167771
MSV3drs167771
GWAS Ctlgrs167771
GMAF0.348
Max Magnitude1.1
? (A;A) (A;G) (G;G) 28


[PMID 19058789] rs167771 was significantly associated with autism spectrum disorder in a study of 144 patients.

[PMID 19506579] G allele associated with increased extra-pyramidal symptom risk as a result of risperidone treatment in a study of 321 psychiatric inpatients (81 presenting with EPS and 189 without)


[PMID 21691864OA-icon.png] Brief Report: The Dopamine-3-Receptor Gene (DRD3) is Associated with Specific Repetitive Behavior in Autism Spectrum Disorder (ASD)


[PMID 22309839] Association study of 45 candidate genes in nicotine dependence in Han Chinese


[PMID 18330705OA-icon.png] Physiogenomic analysis of localized FMRI brain activity in schizophrenia.


[PMID 20148275OA-icon.png] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.


[PMID 20619616] Searching for functional SNPs or rare variants in exonic regions of DRD3 in risperidone-treated patients.


[PMID 22397633] Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.


[PMID 25792691] DRD3 gene and striatum in autism spectrum disorder


[PMID 33204361OA-icon.png] Facial Emotion Recognition and Polymorphisms of Dopaminergic Pathway Genes in Children with ASD.