{{Rsnum
|rsid=11845632
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NRXN3
|position=79487471
|Gene_s=NRXN3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.0 | 54.9 | 30.1
| HCB | 13.1 | 48.9 | 38.0
| JPT | 15.0 | 46.0 | 38.9
| YRI | 89.8 | 10.2 | 0.0
| ASW | 57.9 | 36.8 | 5.3
| CHB | 13.1 | 48.9 | 38.0
| CHD | 18.3 | 52.3 | 29.4
| GIH | 28.7 | 51.5 | 19.8
| LWK | 76.4 | 22.7 | 0.9
| MEX | 10.3 | 36.2 | 53.4
| MKK | 73.1 | 25.0 | 1.9
| TSI | 16.7 | 48.0 | 35.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24265751
|Title=DNA pooling base genome-wide association study identifies variants at NRXN3 associated with delayed encephalopathy after acute carbon monoxide poisoning
}}

{{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}}