rs2097603
From SNPedia
| Merged into | rs2075507 |
| Orientation | plus |
| Stabilized | plus |
| Make rs2097603(A;A) |
| Make rs2097603(A;G) |
| Make rs2097603(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19940569 |
| Gene | COMT, TXNRD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2097603 |
| dbSNP (classic) | rs2097603 |
| ClinGen | rs2097603 |
| ebi | rs2097603 |
| HLI | rs2097603 |
| Exac | rs2097603 |
| Gnomad | rs2097603 |
| Varsome | rs2097603 |
| LitVar | rs2097603 |
| Map | rs2097603 |
| PheGenI | rs2097603 |
| Biobank | rs2097603 |
| 1000 genomes | rs2097603 |
| hgdp | rs2097603 |
| ensembl | rs2097603 |
| geneview | rs2097603 |
| scholar | rs2097603 |
| rs2097603 | |
| pharmgkb | rs2097603 |
| gwascentral | rs2097603 |
| openSNP | rs2097603 |
| 23andMe | rs2097603 |
| SNPshot | rs2097603 |
| SNPdbe | rs2097603 |
| MSV3d | rs2097603 |
| GWAS Ctlg | rs2097603 |
| Status | Merged into rs2075507 |
| Max Magnitude | 0 |
[PMID 19071221
] gray matter volume and interacts with rs2097603 related to extracellular dopamine
[PMID 19605537] Effects of Catechol-O-Methyltransferase on Normal Variation in the Cognitive Function of Children
[PMID 24862404] Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children
