DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799732
rs1799732
Entrez Id: 1813;105369501
Gene Symbol: DRD2;LOC105369501
DRD2;LOC105369501
CUI: C0036341
Disease:
Schizophrenia
0.050 GeneticVariation BEFREE The -141C Ins/Del polymorphism in DRD2 (rs1799732) is functional and associated with SCZ. 31176829 2019
dbSNP: rs1799732
rs1799732
Entrez Id: 1813;105369501
Gene Symbol: DRD2;LOC105369501
DRD2;LOC105369501
CUI: C0036341
Disease:
Schizophrenia
0.050 GeneticVariation BEFREE A single nucleotide polymorphism, -141C insertion/deletion (Ins/Del) (rs1799732), in the promoter region of the dopamine D2 receptor gene has been linked to schizophrenia; however, the data are inconclusive. 26346037 2016
dbSNP: rs1799732
rs1799732
Entrez Id: 1813;105369501
Gene Symbol: DRD2;LOC105369501
DRD2;LOC105369501
CUI: C0036341
Disease:
Schizophrenia
0.050 GeneticVariation BEFREE No significant associations were observed between rs1799732 and rs1800rs732 and rs1800497 and schizophrenia. 25504812 2015
dbSNP: rs1799732
rs1799732
Entrez Id: 1813;105369501
Gene Symbol: DRD2;LOC105369501
DRD2;LOC105369501
CUI: C0036341
Disease:
Schizophrenia
0.050 GeneticVariation BEFREE Thus the aim of the present study was to investigate the possible association between the -141 Ins/Del (rs1799732) polymorphism of the dopamine receptor type 2 (DRD2) and schizophrenia. 19547807 2009
dbSNP: rs1799732
rs1799732
Entrez Id: 1813;105369501
Gene Symbol: DRD2;LOC105369501
DRD2;LOC105369501
CUI: C0036341
Disease:
Schizophrenia
0.050 GeneticVariation BEFREE To test the hypothesis that DRD2 polymorphisms are associated with schizophrenia, we investigated two DRD2-related polymorphisms (TaqI A1/A2 or rs1800497 and -141-C Ins/Del or rs1799732) in a Spanish population isolate from northern Spain consisting of 165 controls and 119 patients with schizophrenia. 17417059 2007