rs5993882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5993882(G;G) |
| Make rs5993882(G;T) |
| Make rs5993882(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19950010 |
| Gene | COMT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5993882 |
| dbSNP (classic) | rs5993882 |
| ClinGen | rs5993882 |
| ebi | rs5993882 |
| HLI | rs5993882 |
| Exac | rs5993882 |
| Gnomad | rs5993882 |
| Varsome | rs5993882 |
| LitVar | rs5993882 |
| Map | rs5993882 |
| PheGenI | rs5993882 |
| Biobank | rs5993882 |
| 1000 genomes | rs5993882 |
| hgdp | rs5993882 |
| ensembl | rs5993882 |
| geneview | rs5993882 |
| scholar | rs5993882 |
| rs5993882 | |
| pharmgkb | rs5993882 |
| gwascentral | rs5993882 |
| openSNP | rs5993882 |
| 23andMe | rs5993882 |
| SNPshot | rs5993882 |
| SNPdbe | rs5993882 |
| MSV3d | rs5993882 |
| GWAS Ctlg | rs5993882 |
| GMAF | 0.2433 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
This is one of the SNPs reported by NutraHacker.
[PMID 16848906
] Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 19772600] A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.
[PMID 22337325] The effect of catechol-O-methyltransferase polymorphisms on pain is modified by depressive symptoms.
