rs1051009
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1051009(C;C) |
| Make rs1051009(C;T) |
| Make rs1051009(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 4734591 |
| Gene | CXCL16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1051009 |
| dbSNP (classic) | rs1051009 |
| ClinGen | rs1051009 |
| ebi | rs1051009 |
| HLI | rs1051009 |
| Exac | rs1051009 |
| Gnomad | rs1051009 |
| Varsome | rs1051009 |
| LitVar | rs1051009 |
| Map | rs1051009 |
| PheGenI | rs1051009 |
| Biobank | rs1051009 |
| 1000 genomes | rs1051009 |
| hgdp | rs1051009 |
| ensembl | rs1051009 |
| geneview | rs1051009 |
| scholar | rs1051009 |
| rs1051009 | |
| pharmgkb | rs1051009 |
| gwascentral | rs1051009 |
| openSNP | rs1051009 |
| 23andMe | rs1051009 |
| SNPshot | rs1051009 |
| SNPdbe | rs1051009 |
| MSV3d | rs1051009 |
| GWAS Ctlg | rs1051009 |
| GMAF | 0.3163 |
| 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
[PMID 19503741
] Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 19753309] SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 20157514] Positive association of common variants in CD36 with neovascular age-related macular degeneration.
