rs1173771
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1173771(C;C) |
| Make rs1173771(C;T) |
| Make rs1173771(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 32814922 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1173771 |
| dbSNP (classic) | rs1173771 |
| ClinGen | rs1173771 |
| ebi | rs1173771 |
| HLI | rs1173771 |
| Exac | rs1173771 |
| Gnomad | rs1173771 |
| Varsome | rs1173771 |
| LitVar | rs1173771 |
| Map | rs1173771 |
| PheGenI | rs1173771 |
| Biobank | rs1173771 |
| 1000 genomes | rs1173771 |
| hgdp | rs1173771 |
| ensembl | rs1173771 |
| geneview | rs1173771 |
| scholar | rs1173771 |
| rs1173771 | |
| pharmgkb | rs1173771 |
| gwascentral | rs1173771 |
| openSNP | rs1173771 |
| 23andMe | rs1173771 |
| SNPshot | rs1173771 |
| SNPdbe | rs1173771 |
| MSV3d | rs1173771 |
| GWAS Ctlg | rs1173771 |
| GMAF | 0.3453 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21909115 ]
|
| Trait | |
| Title | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
| Risk Allele | G |
| P-val | 9E-12 |
| Odds Ratio | 0.2610 [NR] mmHg increase |
| GWAS snp | |
|---|---|
| PMID | [PMID 21909110]
|
| Trait | |
| Title | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. |
| Risk Allele | G |
| P-val | 4E-9 |
| Odds Ratio | 0.2830 [0.19-0.37] mmHg increase |
[PMID 22504314] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
