{{Rsnum
|rsid=1423096
|Chromosome=19
|position=7674291
|Orientation=minus
|GMAF=0.1074
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 21.2 | 77.9
| HCB | 2.9 | 36.5 | 60.6
| JPT | 1.8 | 33.6 | 64.6
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 17.5 | 82.5
| CHB | 2.9 | 36.5 | 60.6
| CHD | 7.3 | 28.4 | 64.2
| GIH | 0.0 | 11.9 | 88.1
| LWK | 0.0 | 5.5 | 94.5
| MEX | 0.0 | 10.7 | 89.3
| MKK | 0.0 | 9.6 | 90.4
| TSI | 0.0 | 15.7 | 84.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=24123702
|Title=Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: A Mendelian randomization effect
}}

{{PMID Auto
|PMID=19074981
|Title=Association of variants in RETN with plasma resistin levels and diabetes-related traits in the Framingham Offspring Study.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}