{{Rsnum
|rsid=1051009
|Gene=CXCL16
|Chromosome=17
|position=4734591
|Orientation=minus
|GMAF=0.3163
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CXCL16
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 48.7 | 41.6 | 9.7
| HCB | 24.1 | 51.8 | 24.1
| JPT | 20.4 | 53.1 | 26.5
| YRI | 100.0 | 0.0 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 24.1 | 51.8 | 24.1
| CHD | 23.9 | 54.1 | 22.0
| GIH | 41.6 | 51.5 | 6.9
| LWK | 99.1 | 0.9 | 0.0
| MEX | 41.4 | 46.6 | 12.1
| MKK | 95.5 | 4.5 | 0.0
| TSI | 35.3 | 52.9 | 11.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=19954776
|Title=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 Auto
|PMID=19503741
|Title=Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=19753309
|Title=SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=20157514
|Title=Positive association of common variants in CD36 with neovascular age-related macular degeneration.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}