rs1801028, DRD2

N. diseases: 24
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Delusions
CUI: C0011253
Disease: Delusions
0.020 GeneticVariation BEFREE When we considered the 887 subjects with the symptomatologic analysis, we observed a significant association of the DRD2 S311C variant with both delusion and disorganization features. 10889529 2000
Delusions
CUI: C0011253
Disease: Delusions
0.020 GeneticVariation BEFREE These data suggest that S311C might be one of the genetic factors for symptomatic dimensions of delusions and hallucinations and might be involved in underlying clinical heterogeneity in schizophrenia and affective disorders. 8723039 1996