rs740603
| Orientation | plus |
| Stabilized | plus |
| Make rs740603(A;A) |
| Make rs740603(A;G) |
| Make rs740603(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19957654 |
| Gene | COMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs740603 |
| dbSNP (classic) | rs740603 |
| ClinGen | rs740603 |
| ebi | rs740603 |
| HLI | rs740603 |
| Exac | rs740603 |
| Gnomad | rs740603 |
| Varsome | rs740603 |
| LitVar | rs740603 |
| Map | rs740603 |
| PheGenI | rs740603 |
| Biobank | rs740603 |
| 1000 genomes | rs740603 |
| hgdp | rs740603 |
| ensembl | rs740603 |
| geneview | rs740603 |
| scholar | rs740603 |
| rs740603 | |
| pharmgkb | rs740603 |
| gwascentral | rs740603 |
| openSNP | rs740603 |
| 23andMe | rs740603 |
| SNPshot | rs740603 |
| SNPdbe | rs740603 |
| MSV3d | rs740603 |
| GWAS Ctlg | rs740603 |
| GMAF | 0.4738 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23269216] Association between the COMT gene and rumination in a Hungarian sample
[PMID 16395295] Significant association of catechol-O-methyltransferase (COMT) haplotypes with nicotine dependence in male and female smokers of two ethnic populations.
[PMID 16848906
] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
[PMID 18436194] Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes.
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
[PMID 19094200] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.
[PMID 19673036] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.
[PMID 19693267] Financial and psychological risk attitudes associated with two single nucleotide polymorphisms in the nicotine receptor (CHRNA4) gene.
[PMID 19772600] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.
[PMID 21656904] Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.
[PMID 22354729] Association of catechol-O-methyltransferase gene polymorphisms with schizophrenia and negative symptoms in a Chinese population.
[PMID 23008195] Genetic variants in the catechol-o-methyltransferase gene are associated with impulsivity and executive function: relevance for major depression.
[PMID 26233486] Variations in opioid receptor genes in neonatal abstinence syndrome
