{{Rsnum
|rsid=2075507
|Gene=TXNRD2
|Chromosome=22
|position=19940569
|Orientation=plus
|GMAF=0.3545
|Gene_s=COMT,TXNRD2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{PMID Auto
|PMID=19605537
|Title=Effects of Catechol-O-Methyltransferase on Normal Variation in the Cognitive Function of Children
|OA=1
}}

{{PMID Auto
|PMID=21595525
|Title=Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder
}}

{{PMID Auto
|PMID=21940152
|Title=The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder - A European Multicenter Study
}}
{{PMID Auto
|PMID=15457404
|Title=Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
|OA=1
}}

{{PMID Auto
|PMID=16232322
|Title=COMT genetic variation confers risk for psychotic and affective disorders: a case control study.
|OA=1
}}

{{PMID Auto
|PMID=16786032
|Title=Impact of complex genetic variation in COMT on human brain function.
}}

{{PMID Auto
|PMID=17006672
|Title=Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.
}}

{{PMID Auto
|PMID=17482701
|Title=No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.
}}

{{PMID Auto
|PMID=17504246
|Title=Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
}}

{{PMID Auto
|PMID=17707347
|Title=Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.
|OA=1
}}

{{PMID Auto
|PMID=17949513
|Title=Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
}}

{{PMID Auto
|PMID=18064318
|Title=Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk.
}}

{{PMID Auto
|PMID=18408230
|Title=Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"?
|OA=1
}}

{{PMID Auto
|PMID=18574484
|Title=The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
|OA=1
}}

{{PMID Auto
|PMID=19071221
|Title=Impact of interacting functional variants in COMT on regional gray matter volume in human brain.
|OA=1
}}

{{PMID Auto
|PMID=19094200
|Title=Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.
|OA=1
}}

{{PMID Auto
|PMID=19329282
|Title=Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.
}}

{{PMID Auto
|PMID=19365560
|Title=Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.
|OA=1
}}

{{PMID Auto
|PMID=20080926
|Title=The influence of 5-HTT and COMT genotypes on verbal fluency in ecstasy users.
}}

{{PMID Auto
|PMID=20531207
|Title=The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
}}

{{PMID Auto
|PMID=21462137
|Title=[An association study of COMT gene polymorphisms with schizophrenia].
}}

{{on chip | 23andMe v3}}