rs2075507
| Orientation | plus |
| Stabilized | plus |
| Make rs2075507(A;A) |
| Make rs2075507(A;G) |
| Make rs2075507(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19940569 |
| Gene | COMT, TXNRD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2075507 |
| dbSNP (classic) | rs2075507 |
| ClinGen | rs2075507 |
| ebi | rs2075507 |
| HLI | rs2075507 |
| Exac | rs2075507 |
| Gnomad | rs2075507 |
| Varsome | rs2075507 |
| LitVar | rs2075507 |
| Map | rs2075507 |
| PheGenI | rs2075507 |
| Biobank | rs2075507 |
| 1000 genomes | rs2075507 |
| hgdp | rs2075507 |
| ensembl | rs2075507 |
| geneview | rs2075507 |
| scholar | rs2075507 |
| rs2075507 | |
| pharmgkb | rs2075507 |
| gwascentral | rs2075507 |
| openSNP | rs2075507 |
| 23andMe | rs2075507 |
| SNPshot | rs2075507 |
| SNPdbe | rs2075507 |
| MSV3d | rs2075507 |
| GWAS Ctlg | rs2075507 |
| Merged from | Rs2097603 |
| GMAF | 0.3545 |
| Max Magnitude | 0 |
[PMID 19605537
] 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 15457404] Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
[PMID 16232322] 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 17707347] 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 18408230] Structural cerebral variations as useful endophenotypes in schizophrenia: do they help construct "extended endophenotypes"?
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 19071221] Impact of interacting functional variants in COMT on regional gray matter volume in human brain.
[PMID 19094200] 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 19365560] 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.
