rs16849225
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16849225(C;C) |
| Make rs16849225(C;T) |
| Make rs16849225(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 164050310 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16849225 |
| dbSNP (classic) | rs16849225 |
| ClinGen | rs16849225 |
| ebi | rs16849225 |
| HLI | rs16849225 |
| Exac | rs16849225 |
| Gnomad | rs16849225 |
| Varsome | rs16849225 |
| LitVar | rs16849225 |
| Map | rs16849225 |
| PheGenI | rs16849225 |
| Biobank | rs16849225 |
| 1000 genomes | rs16849225 |
| hgdp | rs16849225 |
| ensembl | rs16849225 |
| geneview | rs16849225 |
| scholar | rs16849225 |
| rs16849225 | |
| pharmgkb | rs16849225 |
| gwascentral | rs16849225 |
| openSNP | rs16849225 |
| 23andMe | rs16849225 |
| SNPshot | rs16849225 |
| SNPdbe | rs16849225 |
| MSV3d | rs16849225 |
| GWAS Ctlg | rs16849225 |
| GMAF | 0.242 |
| 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 | 4E-11 |
| Odds Ratio | 0.7500 [0.53-0.97] mm Hg increase |
