{{Rsnum
|rsid=701428
|Gene=RTN4R
|Chromosome=22
|position=20241019
|Orientation=plus
|GMAF=0.4688
|Gene_s=RTN4R
|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 | 15.0 | 46.0 | 38.9
| HCB | 16.8 | 45.3 | 38.0
| JPT | 31.2 | 42.0 | 26.8
| YRI | 40.8 | 45.6 | 13.6
| ASW | 26.3 | 56.1 | 17.5
| CHB | 16.8 | 45.3 | 38.0
| CHD | 13.8 | 54.1 | 32.1
| GIH | 29.7 | 45.5 | 24.8
| LWK | 37.3 | 48.2 | 14.5
| MEX | 25.9 | 48.3 | 25.9
| MKK | 20.5 | 47.4 | 32.1
| TSI | 12.7 | 52.9 | 34.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24321711
|Title=White matter abnormalities in 22q11.2 deletion syndrome: Preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis
}}

{{PMID Auto
|PMID=19052207
|Title=Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
|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}}