rs483223
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs483223(C;C) |
| Make rs483223(C;T) |
| Make rs483223(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 117299200 |
| Gene | ROS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs483223 |
| dbSNP (classic) | rs483223 |
| ClinGen | rs483223 |
| ebi | rs483223 |
| HLI | rs483223 |
| Exac | rs483223 |
| Gnomad | rs483223 |
| Varsome | rs483223 |
| LitVar | rs483223 |
| Map | rs483223 |
| PheGenI | rs483223 |
| Biobank | rs483223 |
| 1000 genomes | rs483223 |
| hgdp | rs483223 |
| ensembl | rs483223 |
| geneview | rs483223 |
| scholar | rs483223 |
| rs483223 | |
| pharmgkb | rs483223 |
| gwascentral | rs483223 |
| openSNP | rs483223 |
| 23andMe | rs483223 |
| SNPshot | rs483223 |
| SNPdbe | rs483223 |
| MSV3d | rs483223 |
| GWAS Ctlg | rs483223 |
| GMAF | 0.1593 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| Rs483223 | |
|---|---|
| PubMed | [PMID 16175505 ]
|
| Affy Probeset | SNP_A-8674727 |
| Affy Orientation | same |
| On GW 5.0 | 0 |
| Alleles A/B | C/T |
| Ancestral | T |
| Population | Caucasian |
| Allele | T |
| Case Freq. | |
| Control Freq. | |
| Odds Ratio Het | 1.15 |
| Odds Ratio Hom | 1.75 |
| Odds Ratio All | |
| Disease | Myocardial Infarction (MI) |
rs483223 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocardial Infarction 1.15 times for heterozygotes (CT) and 1.75 times for homozygotes (TT) [PMID 16175505]
