rs167771, DRD3

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.030 GeneticVariation BEFREE The rs167771 SNP was recently also found to be related to risperidone-induced extra-pyramidal side effects (EPS) in patients with autism, which is important since risperidone is approved for the treatment of aggression, irritability and rigid behavior in ASD. 25224105 2015
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.030 GeneticVariation BEFREE A single-nucleotide polymorphism (SNP) of the DRD3 gene (rs167771) was recently associated with autism spectrum disorders (ASD). 25792691 2015
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
0.030 GeneticVariation BEFREE However, the rs167771 marker in DRD3, associated with ASD in a previous study, displayed a nominal association in our analysis (P = 0.023). 22397633 2013
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.010 GeneticVariation BEFREE The rs167771 SNP was recently also found to be related to risperidone-induced extra-pyramidal side effects (EPS) in patients with autism, which is important since risperidone is approved for the treatment of aggression, irritability and rigid behavior in ASD. 25224105 2015
Stereotyped behavior (Psychiatry)
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
0.010 GeneticVariation BEFREE The DRD3 polymorphisms of rs167771 are significantly associated with a specific type of repetitive and stereotyped behavior, called sameness. 25224105 2015
Elastosis perforans serpiginosa
CUI: C0221271
Disease: Elastosis perforans serpiginosa
0.010 GeneticVariation BEFREE One SNP of the DRD3 gene, rs167771</span>, achieved significant association with EPS risk after Bonferroni correction (nominal P-value 1.3 x 10(-4)) in the patients treated with risperidone (132 patients). 19506579 2009
EAR, PATELLA, SHORT STATURE SYNDROME
CUI: C1868684
Disease: EAR, PATELLA, SHORT STATURE SYNDROME
0.010 GeneticVariation BEFREE One SNP of the DRD3 gene, rs167771</span>, achieved significant association with EPS risk after Bonferroni correction (nominal P-value 1.3 x 10(-4)) in the patients treated with risperidone (132 patients). 19506579 2009