DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0424101
Disease: Inattention
Inattention
0.030 GeneticVariation phenotype BEFREE Having the DRD2 Taq1A1 allele and OFC predicted fewer (p = .02) inattentive ADHD symptoms. 25271118 2015
CUI: C0424101
Disease: Inattention
Inattention
0.030 GeneticVariation phenotype BEFREE DAT1 intron8 was associated with parent-rated hyperactivity (ηp(2)=.045) and both DAT1 9/10 VNTR (ηp(2)=.105) and DRD2 rs2283265 (ηp(2)=.069) were associated with teacher-rated inattention. 24780147 2014
CUI: C0424101
Disease: Inattention
Inattention
0.030 GeneticVariation phenotype BEFREE The heritability from the DRD2 locus was estimated at 4.27% for hyperactive-impulsive symptoms and 2.12% for inattentive symptoms. 10578241 1999