rs769224
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs769224(A;A) |
| Make rs769224(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19964281 |
| Gene | COMT, MIR4761 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769224 |
| dbSNP (classic) | rs769224 |
| ClinGen | rs769224 |
| ebi | rs769224 |
| HLI | rs769224 |
| Exac | rs769224 |
| Gnomad | rs769224 |
| Varsome | rs769224 |
| LitVar | rs769224 |
| Map | rs769224 |
| PheGenI | rs769224 |
| Biobank | rs769224 |
| 1000 genomes | rs769224 |
| hgdp | rs769224 |
| ensembl | rs769224 |
| geneview | rs769224 |
| scholar | rs769224 |
| rs769224 | |
| pharmgkb | rs769224 |
| gwascentral | rs769224 |
| openSNP | rs769224 |
| 23andMe | rs769224 |
| SNPshot | rs769224 |
| SNPdbe | rs769224 |
| MSV3d | rs769224 |
| GWAS Ctlg | rs769224 |
| GMAF | 0.04729 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19365560
] Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs
[PMID 18574484] The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
[PMID 21680027] Influence and interaction of genetic polymorphisms in catecholamine neurotransmitter systems and early life stress on antidepressant drug response.
[PMID 24174958] Mercury Promotes Catecholamines Which Potentiate Mercurial Autoimmunity and Vasodilation: Implications for Inositol 1,4,5-Triphosphate 3-Kinase C Susceptibility in Kawasaki Syndrome
