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: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE In a cross-sectional study, we examined 2 dopamine D2 receptor (DRD2) single-nucleotide polymorphisms (SNPs) previously associated with schizophrenia (C939 T, rs6275 and C957 T, rs6277) along with fasting blood glucose and body mass index (BMI) in 207 antipsychotic-treated patients with schizophrenia. 27254804 2016
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE No association between C939T polymorphism and schizophrenia was found in overall or Asian population. 25240594 2014
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE Our results demonstrated initial significant associations of two SNPs for DRD2 (rs11608185, genotype: chi(2) = 6.29, p-value = 0.043; rs6275, genotype: chi(2) = 8.91, p-value = 0.011), and one SNP in the COMT gene (rs4680, genotype: chi(2) = 6.67, p-value = 0.035 and allele: chi(2) = 4.75, p-value = 0.029; odds ratio: 1.33, 95% confidence interval: 1.02-1.73), but not after correction for multiple comparisons indicating a weak association of individual markers of DRD2 and COMT with schizophrenia. 19207030 2009
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0036341
Disease:
Schizophrenia
0.040 GeneticVariation BEFREE To replicate and extend previous findings, we conducted an association study of the C957T polymorphism and two additional SNPs (C939T and TaqIA) in 311 patients with a DSM-IV diagnosis of schizophrenia and 364 mentally healthy people from the Russian population as controls. 18255274 2008