From SNPedia
rs6922269 has been reported in a large study to be associated with
heart disease, in particular,
coronary artery disease.
The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.17 (CI 1.04-1.32), and for homozygotes, 1.65 (CI 1.32-2.06). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|
 |
[PMID 19164808] Large scale association analysis of novel genetic loci for coronary artery disease
[PMID 18675980] Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes
| PharmGKB | PA162356675 |
| Name | |
| Annotation | GWAS Results: Genomewide association analysis of coronary artery disease (Initial Sample Size: 1,926 cases, 2,938 controls; Replication Sample Size: 875 cases, 1,644 controls; Risk Allele: rs6922269-A). |
| Gene | MTHFD1L |
| Featue | |
| Evidence | PubMed ID:17634449; Web Resource:http://www.genome.gov/gwastudies/ |
| Drugs | |
| Diseases | Coronary Disease |
| Curation Level | Non-Curated |
