{{Rsnum
|rsid=2196447
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NRXN3
|position=79484145
|Gene_s=NRXN3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 28.3 | 46.9 | 24.8
| HCB | 13.9 | 49.6 | 36.5
| JPT | 12.4 | 47.8 | 39.8
| YRI | 95.9 | 4.1 | 0.0
| ASW | 75.4 | 21.1 | 3.5
| CHB | 13.9 | 49.6 | 36.5
| CHD | 16.5 | 50.5 | 33.0
| GIH | 34.7 | 51.5 | 13.9
| LWK | 86.4 | 12.7 | 0.9
| MEX | 15.5 | 36.2 | 48.3
| MKK | 83.3 | 16.0 | 0.6
| TSI | 24.5 | 48.0 | 27.5
| 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 | FTDNA}}
{{on chip | Illumina Human 1M}}