{{Rsnum
|rsid=2241714
|Gene=B9D2
|Chromosome=19
|position=41363487
|Orientation=minus
|GMAF=0.3489
|Gene_s=B9D2,TMEM91
|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 | 10.6 | 37.2 | 52.2
| HCB | 24.8 | 48.2 | 27.0
| JPT | 20.4 | 50.4 | 29.2
| YRI | 4.1 | 23.8 | 72.1
| ASW | 3.5 | 21.1 | 75.4
| CHB | 24.8 | 48.2 | 27.0
| CHD | 37.6 | 42.2 | 20.2
| GIH | 16.8 | 44.6 | 38.6
| LWK | 1.8 | 26.4 | 71.8
| MEX | 12.3 | 49.1 | 38.6
| MKK | 3.8 | 24.4 | 71.8
| TSI | 17.6 | 44.1 | 38.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=23094028
|Title=Genetic association analysis of complex diseases incorporating intermediate phenotype information
|OA=1
}}

{{PMID Auto
|PMID=18366677
|Title=Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission.
|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}}