{{Rsnum
|rsid=7835688
|Gene=NRG1
|Chromosome=8
|position=32553981
|Orientation=plus
|GMAF=0.3352
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=NRG1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 17.2 | 50.0 | 32.8
| HCB | 2.2 | 24.8 | 73.0
| JPT | 5.4 | 39.3 | 55.4
| YRI | 3.4 | 32.0 | 64.6
| ASW | 7.0 | 36.8 | 56.1
| CHB | 2.2 | 24.8 | 73.0
| CHD | 3.7 | 26.9 | 69.4
| GIH | 19.2 | 50.5 | 30.3
| LWK | 2.7 | 28.2 | 69.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 5.2 | 39.6 | 55.2
| TSI | 16.0 | 56.0 | 28.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19196962
|Title=Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
|OA=1
}}

{{PMID|21283760|OA=1
}} Fine mapping of the NRG1 Hirschsprung's disease locus.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}