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: C0149931
Disease:
Migraine Disorders
0.040 GeneticVariation BEFREE Odd ratios (ORs) with 95% confidence intervals (95% CIs) were used to evaluate the association between the 5 genetic polymorphisms and migraine susceptibility.There was no significant relationship between migraine susceptibility and 4 genetic polymorphisms of DRD2 rs1799732 and rs6275, DBH rs7239728, and MAO-A-VNTR. 26632697 2015
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0149931
Disease:
Migraine Disorders
0.040 GeneticVariation BEFREE By multivariate logistic stepwise regression analysis, type of migraine, regular and sufficient dietary intake, and methylenetetrahydrofolate reductase (MTHFR) C677T (rs1801133) and dopamine D2 receptor (DRD2) C939T (rs6275) polymorphisms were selected as significant factors that contribute independently to the development from migraine to MOH (P < 0.05). 22290307 2013
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0149931
Disease:
Migraine Disorders
0.040 GeneticVariation BEFREE Therefore, we aimed to look for association of functional variants in ANKK1 (rs1800497), DRD2 (rs6275 and rs1799732) and DBH (rs7239728 and rs1611115) genes with migraine susceptibility. 22875483 2013
dbSNP: rs6275
rs6275
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0149931
Disease:
Migraine Disorders
0.040 GeneticVariation BEFREE The multivariate stepwise logistic regression analysis revealed that age, periorbital/deep orbital pain and C/C genotype carrier at DRD2 C939T were significant factors that contributed independently to the negative response to triptans in patients with migraine. 21822697 2012