rs740602
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs740602(A;A) |
| Make rs740602(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 19962745 |
| Gene | COMT, MIR4761 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs740602 |
| dbSNP (classic) | rs740602 |
| ClinGen | rs740602 |
| ebi | rs740602 |
| HLI | rs740602 |
| Exac | rs740602 |
| Gnomad | rs740602 |
| Varsome | rs740602 |
| LitVar | rs740602 |
| Map | rs740602 |
| PheGenI | rs740602 |
| Biobank | rs740602 |
| 1000 genomes | rs740602 |
| hgdp | rs740602 |
| ensembl | rs740602 |
| geneview | rs740602 |
| scholar | rs740602 |
| rs740602 | |
| pharmgkb | rs740602 |
| gwascentral | rs740602 |
| openSNP | rs740602 |
| 23andMe | rs740602 |
| SNPshot | rs740602 |
| SNPdbe | rs740602 |
| MSV3d | rs740602 |
| GWAS Ctlg | rs740602 |
| GMAF | 0.05051 |
| 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.
