{{Rsnum
|rsid=4502156
|Chromosome=15
|position=62090956
|Orientation=plus
|GMAF=0.4431
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 21.2 | 41.6 | 37.2
| HCB | 33.1 | 49.3 | 17.6
| JPT | 24.8 | 53.1 | 22.1
| YRI | 66.7 | 29.3 | 4.1
| ASW | 61.4 | 33.3 | 5.3
| CHB | 33.1 | 49.3 | 17.6
| CHD | 24.8 | 48.6 | 26.6
| GIH | 22.8 | 50.5 | 26.7
| LWK | 58.2 | 34.5 | 7.3
| MEX | 34.5 | 50.0 | 15.5
| MKK | 51.9 | 38.5 | 9.6
| TSI | 10.8 | 43.1 | 46.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21873549
|Trait=None
|Title=Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
|RiskAllele=T
|Pval=4E-20
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}