{{Rsnum
|rsid=2744148
|Chromosome=16
|position=1023552
|Orientation=plus
|GMAF=0.1024
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 66.4 | 31.0 | 2.7
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 68.7 | 27.2 | 4.1
| ASW | 78.9 | 17.5 | 3.5
| CHB | 100.0 | 0.0 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 50.5 | 39.6 | 9.9
| LWK | 80.0 | 18.2 | 1.8
| MEX | 91.4 | 8.6 | 0.0
| MKK | 74.4 | 23.1 | 2.6
| TSI | 61.8 | 36.3 | 2.0
| 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=G
|Pval=8E-8
|OR=1.1200
|ORtxt=[1.10-1.14]
|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 | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}