rs2681472
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs2681472(C;C) |
| Make rs2681472(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 89615182 |
| Gene | ATP2B1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2681472 |
| dbSNP (classic) | rs2681472 |
| ClinGen | rs2681472 |
| ebi | rs2681472 |
| HLI | rs2681472 |
| Exac | rs2681472 |
| Gnomad | rs2681472 |
| Varsome | rs2681472 |
| LitVar | rs2681472 |
| Map | rs2681472 |
| PheGenI | rs2681472 |
| Biobank | rs2681472 |
| 1000 genomes | rs2681472 |
| hgdp | rs2681472 |
| ensembl | rs2681472 |
| geneview | rs2681472 |
| scholar | rs2681472 |
| rs2681472 | |
| pharmgkb | rs2681472 |
| gwascentral | rs2681472 |
| openSNP | rs2681472 |
| 23andMe | rs2681472 |
| SNPshot | rs2681472 |
| SNPdbe | rs2681472 |
| MSV3d | rs2681472 |
| GWAS Ctlg | rs2681472 |
| GMAF | 0.1924 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19430479 ]
|
| Trait | Diastolic Blood Pressure |
| Title | Genome-wide association study of blood pressure and hypertension |
| Risk Allele | A |
| P-val | 1E-9 |
| Odds Ratio | 0.50 [0.34-0.66] mm Hg increase |
[PMID 22229515] Polymorphism near the ATP2B1 gene is associated with hypertension risk in East Asians: A meta-analysis involving 15 909 cases and 18 529 controls
[PMID 21228780] Novel genetic variations associated with salt sensitivity in the Korean population.
[PMID 23036851] Treatment factors rather than genetic variation determine metabolic syndrome in childhood cancer survivors
[PMID 23079715] Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population.
