{{Rsnum
|rsid=2277680
|Gene=CXCL16
|Chromosome=17
|position=4735268
|Orientation=plus
|GMAF=0.4518
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CXCL16
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.9 | 45.1 | 38.9
| HCB | 32.4 | 51.5 | 16.2
| JPT | 35.4 | 49.6 | 15.0
| YRI | 8.3 | 35.4 | 56.2
| ASW | 7.0 | 43.9 | 49.1
| CHB | 32.4 | 51.5 | 16.2
| CHD | 33.9 | 50.5 | 15.6
| GIH | 19.8 | 58.4 | 21.8
| LWK | 10.0 | 45.5 | 44.5
| MEX | 13.8 | 56.9 | 29.3
| MKK | 6.5 | 58.1 | 35.5
| TSI | 26.5 | 49.0 | 24.5
| 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=17848170
|Title=The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.
|OA=1
}}

{{GET Evidence
|gene=CXCL16
|aa_change=Ala200Val
|aa_change_short=A200V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2277680
|overall_frequency_n=4279
|overall_frequency_d=10758
|overall_frequency=0.39775
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=46
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}