{{Rsnum
|rsid=7255066
|Gene=PVR
|Chromosome=19
|position=44642803
|Orientation=plus
|GMAF=0.4614
|Gene_s=PVR
|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 | 3.5 | 40.7 | 55.8
| HCB | 23.5 | 53.7 | 22.8
| JPT | 24.8 | 51.3 | 23.9
| YRI | 84.9 | 13.7 | 1.4
| ASW | 59.6 | 31.6 | 8.8
| CHB | 23.5 | 53.7 | 22.8
| CHD | 25.7 | 49.5 | 24.8
| GIH | 13.9 | 51.5 | 34.7
| LWK | 72.7 | 24.5 | 2.7
| MEX | 1.7 | 44.8 | 53.4
| MKK | 42.9 | 42.9 | 14.1
| TSI | 4.9 | 41.2 | 53.9
| 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=0.000001
|OR=1.0900
|ORtxt=[1.07-1.11]
|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}}