Rs6475606
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs6475606 |
| hapmap | rs6475606 |
| hgdp | rs6475606 |
| ensembl | rs6475606 |
| gopubmed | rs6475606 |
| scholar | rs6475606 |
| rs6475606 | |
| pharmgkb | rs6475606 |
| hgvbaseg2p | rs6475606 |
| medrefsnp | rs6475606 |
| 23andMe | rs6475606 |
| SNP Nexus |
| Chromosome | 9 |
| Orientation | plus |
| Position | 22071849 |
| Genotype | Effect |
|---|---|
| rs6475606(C;C)* | ? |
| rs6475606(C;T)* | ? |
| rs6475606(T;T)* | ? |
| Rs6475606 | |
|---|---|
| PubMed | [PMID 17478681] |
| Affy Probeset | SNP_A-4213421 |
| Affy Orientation | reverse |
| On GW 5.0 | 1 |
| Alleles A/B | A/G |
| Ancestral | T |
| Population | CEU |
| Allele | T |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | 1.30 |
| Odds Ratio Hom | 1.54 |
| Odds Ratio All | 1.23 |
| Disease | Coronary artery disease (CAD) |
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
| Neighbor | rs10116277 |
| Distance | 453 |
rs6475606 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (CT) and 1.54 times for homozygotes (TT) [PMID 17478681]
