{{Rsnum
|rsid=4410871
|Gene=PVT1
|Chromosome=8
|position=127802783
|Orientation=plus
|GMAF=0.2984
|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 | 54.0 | 34.5 | 11.5
| HCB | 40.9 | 46.7 | 12.4
| JPT | 42.5 | 49.6 | 8.0
| YRI | 73.3 | 24.0 | 2.7
| ASW | 68.4 | 28.1 | 3.5
| CHB | 40.9 | 46.7 | 12.4
| CHD | 34.9 | 60.6 | 4.6
| GIH | 58.4 | 35.6 | 5.9
| LWK | 84.5 | 12.7 | 2.7
| MEX | 24.1 | 51.7 | 24.1
| MKK | 65.4 | 31.4 | 3.2
| TSI | 46.1 | 44.1 | 9.8
| 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=8E-9
|OR=1.1100
|ORtxt=[1.09-1.12]
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23817571
  |Trait=Allergic sensitization
  |Title=Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.
  |RiskAllele=T
  |Pval=5E-10
  |OR=1.14
  |ORtxt=[1.09-1.19]
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}