{{Rsnum
|rsid=17411949
|Gene=CLSTN2
|Chromosome=3
|position=140380851
|Orientation=plus
|GMAF=0.04591
|Gene_s=CLSTN2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 86.7 | 12.4 | 0.9
| HCB | 87.6 | 11.7 | 0.7
| JPT | 93.8 | 5.3 | 0.9
| YRI | 91.8 | 6.8 | 1.4
| ASW | 94.7 | 5.3 | 0.0
| CHB | 87.6 | 11.7 | 0.7
| CHD | 89.0 | 11.0 | 0.0
| GIH | 94.1 | 5.9 | 0.0
| LWK | 89.1 | 10.9 | 0.0
| MEX | 93.1 | 6.9 | 0.0
| MKK | 82.1 | 17.3 | 0.6
| TSI | 89.2 | 10.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23472185
  |Trait=Multiple sclerosis (OCB status)
  |Title=Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
  |RiskAllele=
  |Pval=8E-7
  |OR=1.85
  |ORtxt=[1.45-2.37]
  |OA=1
}}

{{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}}