{{Rsnum
|rsid=354033
|Gene=ZNF767
|Chromosome=7
|position=149592373
|Orientation=minus
|GMAF=0.2025
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ZNF767P
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 60.2 | 32.7 | 7.1
| HCB | 78.8 | 21.2 | 0.0
| JPT | 72.6 | 26.5 | 0.9
| YRI | 60.5 | 36.1 | 3.4
| ASW | 63.2 | 33.3 | 3.5
| CHB | 78.8 | 21.2 | 0.0
| CHD | 82.6 | 16.5 | 0.9
| GIH | 59.4 | 31.7 | 8.9
| LWK | 58.2 | 38.2 | 3.6
| MEX | 70.7 | 24.1 | 5.2
| MKK | 66.7 | 29.5 | 3.8
| TSI | 44.1 | 47.1 | 8.8
| 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=5E-9
|OR=1.1100
|ORtxt=[1.10-1.13]
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}