{{Rsnum
|rsid=6952809
|Gene=CHST12
|Chromosome=7
|position=2408858
|Orientation=plus
|GMAF=0.3136
|Gene_s=CHST12
|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 | 40.7 | 48.7 | 10.6
| HCB | 66.7 | 30.4 | 3.0
| JPT | 61.9 | 34.5 | 3.5
| YRI | 30.8 | 47.9 | 21.2
| ASW | 24.6 | 56.1 | 19.3
| CHB | 66.7 | 30.4 | 3.0
| CHD | 63.0 | 32.4 | 4.6
| GIH | 45.5 | 43.6 | 10.9
| LWK | 37.3 | 45.5 | 17.3
| MEX | 53.4 | 36.2 | 10.3
| MKK | 47.4 | 44.9 | 7.7
| TSI | 47.1 | 41.2 | 11.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=A
  |Pval=4E-6
  |OR=1.08
  |ORtxt=[1.06-1.09]
  |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}}