{{Rsnum
|rsid=4790333
|Gene=SGSM2
|Chromosome=17
|position=2359409
|Orientation=plus
|GMAF=0.4835
|Gene_s=SGSM2
|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 | 37.2 | 46.0 | 16.8
| HCB | 12.4 | 34.3 | 53.3
| JPT | 2.7 | 22.1 | 75.2
| YRI | 47.6 | 45.6 | 6.8
| ASW | 38.6 | 40.4 | 21.1
| CHB | 12.4 | 34.3 | 53.3
| CHD | 7.3 | 38.5 | 54.1
| GIH | 5.0 | 48.5 | 46.5
| LWK | 47.3 | 42.7 | 10.0
| MEX | 37.9 | 48.3 | 13.8
| MKK | 46.2 | 41.7 | 12.2
| TSI | 35.3 | 52.9 | 11.8
| 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=3E-9
|OR=None
|ORtxt=None
|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 | Illumina Human 1M}}