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rs2075507

From SNPedia

Orientationplus
Stabilizedplus
Make rs2075507(A;A)
Make rs2075507(A;G)
Make rs2075507(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position19940569
GeneCOMT, TXNRD2
is asnp
is mentioned by
dbSNPrs2075507
ebirs2075507
HLIrs2075507
Exacrs2075507
Varsomers2075507
Maprs2075507
PheGenIrs2075507
hapmaprs2075507
1000 genomesrs2075507
hgdprs2075507
ensemblrs2075507
gopubmedrs2075507
geneviewrs2075507
scholarrs2075507
googlers2075507
pharmgkbrs2075507
gwascentralrs2075507
openSNPrs2075507
23andMers2075507
23andMe allrs2075507
SNP Nexus

SNPshotrs2075507
SNPdbers2075507
MSV3drs2075507
GWAS Ctlgrs2075507
Merged fromRs2097603
GMAF0.3545
Max Magnitude

[PMID 19605537OA-icon.png] Effects of Catechol-O-Methyltransferase on Normal Variation in the Cognitive Function of Children


[PMID 21595525] Sensory gating deficit is associated with catechol-O-methyltransferase polymorphisms in bipolar disorder


[PMID 21940152] The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder - A European Multicenter Study

[PMID 15457404OA-icon.png] Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.


[PMID 16232322OA-icon.png] COMT genetic variation confers risk for psychotic and affective disorders: a case control study.


[PMID 16786032] Impact of complex genetic variation in COMT on human brain function.


[PMID 17006672] Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia.


[PMID 17482701] No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.


[PMID 17504246] Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.


[PMID 17707347OA-icon.png] Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.


[PMID 17949513] Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.


[PMID 18064318] Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk.


[PMID 18408230OA-icon.png] Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"?


[PMID 18574484OA-icon.png] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.


[PMID 19071221OA-icon.png] Impact of interacting functional variants in COMT on regional gray matter volume in human brain.


[PMID 19094200OA-icon.png] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.


[PMID 19329282] Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.


[PMID 19365560OA-icon.png] Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.


[PMID 20080926] The influence of 5-HTT and COMT genotypes on verbal fluency in ecstasy users.


[PMID 20531207] The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.


[PMID 21462137] [An association study of COMT gene polymorphisms with schizophrenia].


[PMID 27228319] A Tetra-Primer Amplification Refractory System Technique for the Cost-Effective and Novel Genotyping of Eight Single-Nucleotide Polymorphisms of the Catechol-O-Methyltransferase Gene.