From SNPedia
rs2398162 has been reported in a large study to be associated with high blood pressure.
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 0.97 (CI 0.76-1.25), and for homozygotes, 1.31 (CI 1.03-1.67). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|
 |
| GWAS
|
| SNP
| rs2398162
|
| PubMedID
| [PMID 17554300]
|
| Condition
| Hypertension
|
| Gene
| NR
|
| Risk Allele
| A
|
| pValue
| 6.00E-006
|
| OR
| 1.31
|
| 95% CI
| 1.03-1.67
|
| PharmGKB | PA162356647 |
| Name | |
| Annotation | GWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,952 cases, 2,938 controls; Replication Sample Size: NR; Risk Allele: rs2398162-A). This variant is associated with hypertension. |
| Gene | - |
| Featue | |
| Evidence | PubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/ |
| Drugs | |
| Diseases | Hypertension |
| Curation Level | Non-Curated |
