rs6269
| Orientation | plus |
| Stabilized | plus |
| Make rs6269(A;A) |
| Make rs6269(A;G) |
| Make rs6269(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19962429 |
| Gene | COMT, MIR4761 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6269 |
| dbSNP (classic) | rs6269 |
| ClinGen | rs6269 |
| ebi | rs6269 |
| HLI | rs6269 |
| Exac | rs6269 |
| Gnomad | rs6269 |
| Varsome | rs6269 |
| LitVar | rs6269 |
| Map | rs6269 |
| PheGenI | rs6269 |
| Biobank | rs6269 |
| 1000 genomes | rs6269 |
| hgdp | rs6269 |
| ensembl | rs6269 |
| geneview | rs6269 |
| scholar | rs6269 |
| rs6269 | |
| pharmgkb | rs6269 |
| gwascentral | rs6269 |
| openSNP | rs6269 |
| 23andMe | rs6269 |
| SNPshot | rs6269 |
| SNPdbe | rs6269 |
| MSV3d | rs6269 |
| GWAS Ctlg | rs6269 |
| GMAF | 0.3719 |
| Max Magnitude | 0 |
[PMID 19290789] Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment
[PMID 19605537
] Effects of Catechol-O-Methyltransferase on Normal Variation in the Cognitive Function of Children
[PMID 20570835] No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain
[PMID 21300128] COMT Val158met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa
[PMID 21884617] Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults
[PMID 21940152] The impact of COMT gene polymorphisms on suicidality in treatment resistant major depressive disorder - A European Multicenter Study
[PMID 22451510] Catechol-O-Methyltransferase Gene and Executive Function in Children With ADHD
[PMID 22528689] Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene
[PMID 22178088] Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome
[PMID 16848906] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
[PMID 17961261] Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 18698234] The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.
[PMID 18802928] Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.
[PMID 19094200] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.
[PMID 19193196] Genetic contributions to pain: a review of findings in humans.
[PMID 19772600] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.
[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 20627703] The association of single nucleotide polymorphisms in the catechol-O-methyltransferase gene and pain scores in female patients with major depressive disorder.
[PMID 20842020] Catecholamine-o-methyltransferase polymorphisms are associated with postoperative pain intensity.
[PMID 20863768] Association of catechol-O-methyltransferase genetic variants with outcome in patients undergoing surgical treatment for lumbar degenerative disc disease.
[PMID 21304959] Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia.
[PMID 21355050] A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2).
[PMID 21423693] Effect sizes in experimental pain produced by gender, genetic variants and sensitization procedures.
[PMID 21462137] [An association study of COMT gene polymorphisms with schizophrenia].
[PMID 22890010] Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
[PMID 23178897] The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence.
[PMID 24593143] Genetic polymorphisms of catechol-O-methyltransferase modify the neurobehavioral effects of mercury in children
[PMID 26849490] Association between catechol-O-methyl transferase gene polymorphisms and fibromyalgia in a Korean population: A case-control study.
[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.
[PMID 28451382] Roles of functional catechol-O-methyltransferase genotypes in Chinese patients with Parkinson's disease.
[PMID 29559808] Association of genetic variation in COMT gene with pain related to sickle cell disease in patients from the walk-PHaSST study.
[PMID 29330410] The Impact of COMT and Childhood Maltreatment on Suicidal Behaviour in Affective Disorders.
[PMID 33400997] Sensory and psychological factors predict exercise-induced shoulder injury responses in a high-risk phenotype cohort.
