{{Rsnum
|rsid=2059807
|Gene=INSR
|Chromosome=19
|position=7166098
|Orientation=plus
|GMAF=0.449
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=INSR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 34.5 | 48.7 | 16.8
| HCB | 10.2 | 38.7 | 51.1
| JPT | 8.0 | 38.9 | 53.1
| YRI | 63.3 | 34.7 | 2.0
| ASW | 62.5 | 35.7 | 1.8
| CHB | 10.2 | 38.7 | 51.1
| CHD | 12.8 | 44.0 | 43.1
| GIH | 43.6 | 45.5 | 10.9
| LWK | 72.7 | 27.3 | 0.0
| MEX | 25.9 | 44.8 | 29.3
| MKK | 50.6 | 42.9 | 6.4
| TSI | 41.2 | 45.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=21645371
|Title=Family association study between INSR gene polymorphisms and PCOS in Han Chinese
|OA=1
}}

{{PMID|18194558|OA=1
}} A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

{{PMID Auto GWAS
  |PMID=22885925
  |Trait=Polycystic ovary syndrome
  |Title=Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.
  |RiskAllele=G
  |Pval=1E-8
  |OR=1.14
  |ORtxt=[NR]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}