{{Rsnum
|rsid=1531343
|Gene=RPSAP52
|Chromosome=12
|position=65781114
|Orientation=plus
|GMAF=0.1915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=RPSAP52
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 1.8 | 19.5 | 78.8
| HCB | 1.5 | 13.1 | 85.4
| JPT | 3.5 | 17.7 | 78.8
| YRI | 18.4 | 44.2 | 37.4
| ASW | 17.5 | 45.6 | 36.8
| CHB | 1.5 | 13.1 | 85.4
| CHD | 0.9 | 18.3 | 80.7
| GIH | 5.9 | 26.7 | 67.3
| LWK | 29.1 | 52.7 | 18.2
| MEX | 0.0 | 20.7 | 79.3
| MKK | 19.9 | 41.0 | 39.1
| TSI | 3.0 | 28.7 | 68.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20581827
|Trait=Type 2 diabetes
|Title=Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
|RiskAllele=C
|Pval=4E-9
|OR=1.10
|ORtxt=[1.07-1.14]
|OA=1
}}

{{PMID|21278902|OA=1
}} Genetic risk profiling for prediction of type 2 diabetes.

{{PMID Auto
|PMID=23111731
|Title=Common variant in the HMGA2 gene increases susceptibility to nephropathy in patients with type 2 diabetes
}}

{{PMID Auto
|PMID=23462794
|Title=Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}