rs2250333
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2250333(C;C) |
| Make rs2250333(C;T) |
| Make rs2250333(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 4738774 |
| Gene | CXCL16, ZMYND15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2250333 |
| dbSNP (classic) | rs2250333 |
| ClinGen | rs2250333 |
| ebi | rs2250333 |
| HLI | rs2250333 |
| Exac | rs2250333 |
| Gnomad | rs2250333 |
| Varsome | rs2250333 |
| LitVar | rs2250333 |
| Map | rs2250333 |
| PheGenI | rs2250333 |
| Biobank | rs2250333 |
| 1000 genomes | rs2250333 |
| hgdp | rs2250333 |
| ensembl | rs2250333 |
| geneview | rs2250333 |
| scholar | rs2250333 |
| rs2250333 | |
| pharmgkb | rs2250333 |
| gwascentral | rs2250333 |
| openSNP | rs2250333 |
| 23andMe | rs2250333 |
| SNPshot | rs2250333 |
| SNPdbe | rs2250333 |
| MSV3d | rs2250333 |
| GWAS Ctlg | rs2250333 |
| GMAF | 0.2828 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19954776] An intron polymorphism in the CXCL16 gene is associated with increased risk of coronary artery disease in Chinese Han population: A large angiography-based study
