{{Rsnum
|rsid=2303298
|Gene=NRXN1
|Chromosome=2
|position=50623548
|Orientation=plus
|GMAF=0.05601
|Gene_s=NRXN1
|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 | 0.0 | 0.0 | 100.0
| HCB | 0.7 | 17.5 | 81.8
| JPT | 1.8 | 36.3 | 61.9
| YRI | 0.0 | 12.9 | 87.1
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.7 | 17.5 | 81.8
| CHD | 0.9 | 10.1 | 89.0
| GIH | 0.0 | 2.0 | 98.0
| LWK | 0.0 | 16.4 | 83.6
| MEX | 0.0 | 15.5 | 84.5
| MKK | 0.0 | 14.7 | 85.3
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22405623
|Title=Mutation analysis of the NRXN1 gene in a Chinese autism cohort
}}

{{PMID Auto
|PMID=19805132
|Title=Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}