{{Rsnum
|rsid=7405696
|Gene=HNF1B
|Chromosome=17
|position=37742044
|Orientation=plus
|GMAF=0.4059
|Gene_s=HNF1B
|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 | 14.3 | 49.2 | 36.5
| HCB | 35.6 | 48.9 | 15.6
| JPT | 27.3 | 54.5 | 18.2
| YRI | 1.6 | 11.3 | 87.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.6 | 48.9 | 15.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21576123
|Title=Large-scale fine mapping of the HNF1B locus and prostate cancer risk
|OA=1
}}{{PMID|18701471|OA=1
}} Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.