{{Rsnum
|rsid=1549318
|Chromosome=15
|position=70816808
|Orientation=plus
|GMAF=0.455
|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 | 16.8 | 46.9 | 36.3
| HCB | 29.6 | 51.1 | 19.3
| JPT | 20.4 | 54.9 | 24.8
| YRI | 39.0 | 41.1 | 19.9
| ASW | 26.3 | 57.9 | 15.8
| CHB | 29.6 | 51.1 | 19.3
| CHD | 34.3 | 50.0 | 15.7
| GIH | 17.8 | 50.5 | 31.7
| LWK | 37.3 | 45.5 | 17.3
| MEX | 6.9 | 24.1 | 69.0
| MKK | 28.8 | 44.9 | 26.3
| TSI | 9.8 | 46.1 | 44.1
| 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=2E-10
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}