rs17489268
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17489268(A;A) |
| Make rs17489268(A;T) |
| Make rs17489268(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 19994534 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17489268 |
| dbSNP (classic) | rs17489268 |
| ClinGen | rs17489268 |
| ebi | rs17489268 |
| HLI | rs17489268 |
| Exac | rs17489268 |
| Gnomad | rs17489268 |
| Varsome | rs17489268 |
| LitVar | rs17489268 |
| Map | rs17489268 |
| PheGenI | rs17489268 |
| Biobank | rs17489268 |
| 1000 genomes | rs17489268 |
| hgdp | rs17489268 |
| ensembl | rs17489268 |
| geneview | rs17489268 |
| scholar | rs17489268 |
| rs17489268 | |
| pharmgkb | rs17489268 |
| gwascentral | rs17489268 |
| openSNP | rs17489268 |
| 23andMe | rs17489268 |
| SNPshot | rs17489268 |
| SNPdbe | rs17489268 |
| MSV3d | rs17489268 |
| GWAS Ctlg | rs17489268 |
| GMAF | 0.2443 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs17489268 | |
|---|---|
| PubMed | [PMID 17634449 ]
|
| Affy Probeset | SNP_A-2109814 |
| Affy Orientation | same |
| On GW 5.0 | 1 |
| Alleles A/B | A/T |
| Ancestral | T |
| Population | Caucasian |
| Allele | A |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.25 |
| Disease | Coronary artery disease (CAD) |
rs17489268 increases susceptibility to Coronary artery disease 1.25 times for carriers of the A allele [PMID 17634449]
[PMID 20018038] Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study.
[PMID 20370913] Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data.
