rs1173766
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1173766(C;C) |
| Make rs1173766(C;T) |
| Make rs1173766(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 32804422 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1173766 |
| dbSNP (classic) | rs1173766 |
| ClinGen | rs1173766 |
| ebi | rs1173766 |
| HLI | rs1173766 |
| Exac | rs1173766 |
| Gnomad | rs1173766 |
| Varsome | rs1173766 |
| LitVar | rs1173766 |
| Map | rs1173766 |
| PheGenI | rs1173766 |
| Biobank | rs1173766 |
| 1000 genomes | rs1173766 |
| hgdp | rs1173766 |
| ensembl | rs1173766 |
| geneview | rs1173766 |
| scholar | rs1173766 |
| rs1173766 | |
| pharmgkb | rs1173766 |
| gwascentral | rs1173766 |
| openSNP | rs1173766 |
| 23andMe | rs1173766 |
| SNPshot | rs1173766 |
| SNPdbe | rs1173766 |
| MSV3d | rs1173766 |
| GWAS Ctlg | rs1173766 |
| GMAF | 0.4054 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21572416 ]
|
| Trait | |
| Title | Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. |
| Risk Allele | C |
| P-val | 2E-8 |
| Odds Ratio | 0.6300 [0.41-0.85] mm Hg increase |
