{{Rsnum
|rsid=2439305
|Gene=NRG1
|Chromosome=8
|position=32571946
|Orientation=minus
|GMAF=0.4017
|Gene_s=NRG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 24.1 | 45.5 | 30.4
| HCB | 2.2 | 24.8 | 73.0
| JPT | 5.3 | 38.1 | 56.6
| YRI | 21.8 | 49.0 | 29.3
| ASW | 19.3 | 56.1 | 24.6
| CHB | 2.2 | 24.8 | 73.0
| CHD | 3.7 | 27.1 | 69.2
| GIH | 20.8 | 50.5 | 28.7
| LWK | 21.8 | 50.9 | 27.3
| MEX | 25.9 | 53.4 | 20.7
| MKK | 16.0 | 53.8 | 30.1
| TSI | 15.8 | 57.4 | 26.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22377709
|Title=Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}