{{Rsnum
|rsid=891088
|Gene=INSR
|Chromosome=19
|position=7184751
|Orientation=plus
|GMAF=0.3007
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=INSR
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 54.9 | 38.1 | 7.1
| HCB | 69.3 | 28.5 | 2.2
| JPT | 58.4 | 37.2 | 4.4
| YRI | 28.6 | 52.4 | 19.0
| ASW | 35.1 | 40.4 | 24.6
| CHB | 69.3 | 28.5 | 2.2
| CHD | 62.4 | 29.4 | 8.3
| GIH | 33.7 | 45.5 | 20.8
| LWK | 18.2 | 55.5 | 26.4
| MEX | 51.7 | 36.2 | 12.1
| MKK | 22.4 | 49.4 | 28.2
| TSI | 50.0 | 39.2 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20881960
|Trait=None
|Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
|RiskAllele=A
|Pval=2E-12
|OR=0.0300
|ORtxt=[NR] meters decrease
|OA=1
}}

{{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}}