rs7613868
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7613868(C;C) |
| Make rs7613868(C;T) |
| Make rs7613868(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 124023182 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7613868 |
| dbSNP (classic) | rs7613868 |
| ClinGen | rs7613868 |
| ebi | rs7613868 |
| HLI | rs7613868 |
| Exac | rs7613868 |
| Gnomad | rs7613868 |
| Varsome | rs7613868 |
| LitVar | rs7613868 |
| Map | rs7613868 |
| PheGenI | rs7613868 |
| Biobank | rs7613868 |
| 1000 genomes | rs7613868 |
| hgdp | rs7613868 |
| ensembl | rs7613868 |
| geneview | rs7613868 |
| scholar | rs7613868 |
| rs7613868 | |
| pharmgkb | rs7613868 |
| gwascentral | rs7613868 |
| openSNP | rs7613868 |
| 23andMe | rs7613868 |
| SNPshot | rs7613868 |
| SNPdbe | rs7613868 |
| MSV3d | rs7613868 |
| GWAS Ctlg | rs7613868 |
| GMAF | 0.4949 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs7613868 | |
|---|---|
| PubMed | [PMID 17357071 ]
|
| Affy Probeset | SNP_A-8580439 |
| Affy Orientation | same |
| On GW 5.0 | 0 |
| Alleles A/B | C/T |
| Ancestral | T |
| Population | Caucasian |
| Allele | T |
| Case Freq. | 0.37 |
| Control Freq. | 0.26 |
| Odds Ratio Het | |
| Odds Ratio Hom | |
| Odds Ratio All | 1.80 |
| Disease | Coronary artery disease (CAD) |
rs7613868 increases susceptibility to Atherosclerosis 2.60 times for carriers of the T allele [PMID 17357071]
rs7613868 increases susceptibility to Coronary artery disease 1.80 times for carriers of the T allele [PMID 17357071]
