{{Rsnum
|rsid=2119704
|Chromosome=14
|position=88021345
|Orientation=plus
|GMAF=0.1286
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=RP11-300J18.1
|Gene_s=RP11-300J18.1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 11.7 | 87.4
| HCB | 2.2 | 33.3 | 64.4
| JPT | 3.5 | 31.0 | 65.5
| YRI | 3.5 | 34.7 | 61.8
| ASW | 5.3 | 21.1 | 73.7
| CHB | 2.2 | 33.3 | 64.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 7.0 | 92.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 10.7 | 89.3
| MKK | 3.2 | 25.0 | 71.8
| TSI | 1.0 | 18.0 | 81.0
| 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=2E-10
|OR=1.2200
|ORtxt=[1.19-1.25]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}