{{Rsnum
|rsid=630923
|Gene=CXCR5
|Chromosome=11
|position=118883644
|Orientation=plus
|GMAF=0.1065
|Gene_s=CXCR5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 2.7 | 22.1 | 75.2
| HCB | 0.7 | 11.8 | 87.5
| JPT | 0.0 | 5.3 | 94.7
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.7 | 11.8 | 87.5
| CHD | 1.8 | 11.9 | 86.2
| GIH | 0.0 | 20.8 | 79.2
| LWK | 0.0 | 2.7 | 97.3
| MEX | 8.6 | 39.7 | 51.7
| MKK | 0.0 | 3.8 | 96.2
| TSI | 2.0 | 24.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=C
|Pval=3E-7
|OR=1.1200
|ORtxt=[1.10-1.14]
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23128233
  |Trait=Inflammatory bowel disease
  |Title=Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
  |RiskAllele=C
  |Pval=7E-9
  |OR=1.07
  |ORtxt=[1.039-1.11]
  |OA=1
}}

{{PMID Auto
|PMID=23250934
|Title=Serum levels of the chemokine CXCL13, genetic variation in CXCL13 and its receptor CXCR5, and HIV-associated non-hodgkin B-cell lymphoma risk
|OA=1
}}

{{PMID Auto
|PMID=23739915
|Title=MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
}}

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