rs675026
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs675026(C;C) |
| Make rs675026(C;T) |
| Make rs675026(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 154093428 |
| Gene | OPRM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs675026 |
| dbSNP (classic) | rs675026 |
| ClinGen | rs675026 |
| ebi | rs675026 |
| HLI | rs675026 |
| Exac | rs675026 |
| Gnomad | rs675026 |
| Varsome | rs675026 |
| LitVar | rs675026 |
| Map | rs675026 |
| PheGenI | rs675026 |
| Biobank | rs675026 |
| 1000 genomes | rs675026 |
| hgdp | rs675026 |
| ensembl | rs675026 |
| geneview | rs675026 |
| scholar | rs675026 |
| rs675026 | |
| pharmgkb | rs675026 |
| gwascentral | rs675026 |
| openSNP | rs675026 |
| 23andMe | rs675026 |
| SNPshot | rs675026 |
| SNPdbe | rs675026 |
| MSV3d | rs675026 |
| GWAS Ctlg | rs675026 |
| GMAF | 0.2415 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21347282 ]
|
| Trait | |
| Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 1.2000 [1.11-1.30] |
[PMID 19103668] Expansion of the human mu-opioid receptor gene architecture: novel functional variants.
