{{Rsnum
|rsid=2439302
|Gene=NRG1
|Chromosome=8
|position=32574851
|Orientation=minus
|GMAF=0.4013
|Gene_s=NRG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 23.9 | 45.1 | 31.0
| HCB | 2.2 | 25.5 | 72.3
| JPT | 5.3 | 38.1 | 56.6
| YRI | 21.8 | 49.0 | 29.3
| ASW | 19.3 | 56.1 | 24.6
| CHB | 2.2 | 25.5 | 72.3
| CHD | 3.7 | 27.8 | 68.5
| GIH | 20.8 | 50.5 | 28.7
| LWK | 21.8 | 50.9 | 27.3
| MEX | 24.1 | 55.2 | 20.7
| MKK | 16.0 | 53.8 | 30.1
| TSI | 16.7 | 56.9 | 26.5
| HapMapRevision=28
}}

{{PMID Auto GWAS
|PMID=22267200
|Trait=None
|Title=Discovery of common variants associated with low TSH levels and thyroid cancer risk.
|RiskAllele=G
|Pval=2E-9
|OR=1.3600
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=23659773
|Title=Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
}}

{{PMID Auto
|PMID=23847140
|Title=Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population
}}

{{PMID Auto
|PMID=24591304
|Title=Significant SNPs have limited prediction ability for thyroid cancer
}}
{{on chip | Affy GenomeWide 6}}