{{Rsnum
|rsid=12278912
|Gene=NRGN
|Chromosome=11
|position=124742263
|Orientation=plus
|GMAF=0.2902
|Gene_s=NRGN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 6.2 | 38.9 | 54.9
| HCB | 1.5 | 31.1 | 67.4
| JPT | 10.6 | 28.3 | 61.1
| YRI | 36.1 | 49.0 | 15.0
| ASW | 24.6 | 52.6 | 22.8
| CHB | 1.5 | 31.1 | 67.4
| CHD | 2.8 | 37.6 | 59.6
| GIH | 2.0 | 32.7 | 65.3
| LWK | 22.7 | 45.5 | 31.8
| MEX | 3.5 | 26.3 | 70.2
| MKK | 26.9 | 51.3 | 21.8
| TSI | 8.8 | 36.3 | 54.9
| 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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}