{{Rsnum
|rsid=2075713
|Gene=VSIG2
|Chromosome=11
|position=124748043
|Orientation=minus
|GMAF=0.1942
|Gene_s=VSIG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 1.8 | 31.0 | 67.3
| HCB | 2.2 | 22.6 | 75.2
| JPT | 5.3 | 22.1 | 72.6
| YRI | 12.9 | 43.5 | 43.5
| ASW | 7.0 | 49.1 | 43.9
| CHB | 2.2 | 22.6 | 75.2
| CHD | 0.0 | 22.2 | 77.8
| GIH | 1.0 | 30.0 | 69.0
| LWK | 6.4 | 44.5 | 49.1
| MEX | 0.0 | 20.7 | 79.3
| MKK | 7.8 | 55.6 | 36.6
| TSI | 3.9 | 32.4 | 63.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22461181
|Title=Functional genetic variation at the NRGN gene and schizophrenia: Evidence from a gene-based case-control study and gene expression analysis
}}

{{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}}