{{Rsnum
|rsid=16879552
|Gene=NRG1
|Chromosome=8
|position=32553698
|Orientation=plus
|GMAF=0.2433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NRG1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 94.7 | 5.3 | 0.0
| HCB | 10.2 | 56.2 | 33.6
| JPT | 11.6 | 45.5 | 42.9
| YRI | 57.8 | 37.4 | 4.8
| ASW | 61.4 | 31.6 | 7.0
| CHB | 10.2 | 56.2 | 33.6
| CHD | 19.4 | 41.7 | 38.9
| GIH | 81.2 | 17.8 | 1.0
| LWK | 51.8 | 40.0 | 8.2
| MEX | 81.0 | 17.2 | 1.7
| MKK | 67.9 | 31.4 | 0.6
| TSI | 95.1 | 4.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19196962
|Title=Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
|OA=1
}}

{{PharmGKB
|RSID=rs16879552
|Name_s=
|Gene_s=NRG1
|Feature=
|Evidence=PubMed ID:19196962; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. (Initial Sample Size: 181 Chinese cases, 346 Chinese controls; Replication Sample Size: 190 Chinese cases, 510 Chinese controls); (Region: 8p12; Reported Gene(s): NRG1; Risk Allele: rs16879552-G); (p-value= 0.00000002).This variant is associated with Hirschsprung's disease.
|Drugs=
|Drug Classes=
|Diseases=Hirschsprung Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739985
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs16879552
|overall_frequency_n=22
|overall_frequency_d=126
|overall_frequency=0.174603
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}