rs2277680
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2277680(A;A) |
| Make rs2277680(A;G) |
| Make rs2277680(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 4735268 |
| Gene | CXCL16 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2277680 |
| dbSNP (classic) | rs2277680 |
| ClinGen | rs2277680 |
| ebi | rs2277680 |
| HLI | rs2277680 |
| Exac | rs2277680 |
| Gnomad | rs2277680 |
| Varsome | rs2277680 |
| LitVar | rs2277680 |
| Map | rs2277680 |
| PheGenI | rs2277680 |
| Biobank | rs2277680 |
| 1000 genomes | rs2277680 |
| hgdp | rs2277680 |
| ensembl | rs2277680 |
| geneview | rs2277680 |
| scholar | rs2277680 |
| rs2277680 | |
| pharmgkb | rs2277680 |
| gwascentral | rs2277680 |
| openSNP | rs2277680 |
| 23andMe | rs2277680 |
| SNPshot | rs2277680 |
| SNPdbe | rs2277680 |
| MSV3d | rs2277680 |
| GWAS Ctlg | rs2277680 |
| GMAF | 0.4518 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[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 17848170
] The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.
[PMID 27069792] Association of NOD1, CXCL16, STAT6 and TLR4 gene polymorphisms with Malaysian patients with Crohn's disease
