rs11953630
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11953630(C;C) |
| Make rs11953630(C;T) |
| Make rs11953630(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 158418394 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11953630 |
| dbSNP (classic) | rs11953630 |
| ClinGen | rs11953630 |
| ebi | rs11953630 |
| HLI | rs11953630 |
| Exac | rs11953630 |
| Gnomad | rs11953630 |
| Varsome | rs11953630 |
| LitVar | rs11953630 |
| Map | rs11953630 |
| PheGenI | rs11953630 |
| Biobank | rs11953630 |
| 1000 genomes | rs11953630 |
| hgdp | rs11953630 |
| ensembl | rs11953630 |
| geneview | rs11953630 |
| scholar | rs11953630 |
| rs11953630 | |
| pharmgkb | rs11953630 |
| gwascentral | rs11953630 |
| openSNP | rs11953630 |
| 23andMe | rs11953630 |
| SNPshot | rs11953630 |
| SNPdbe | rs11953630 |
| MSV3d | rs11953630 |
| GWAS Ctlg | rs11953630 |
| GMAF | 0.2163 |
| 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 | T |
| P-val | 2E-7 |
| Odds Ratio | 0.0520 [NR] % decrease |
[PMID 22504314] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
