{{Rsnum
|rsid=1411766
|Chromosome=13
|position=109599813
|Orientation=minus
|GMAF=0.2089
|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 | 55.8 | 7.1
| HCB | 87.6 | 11.7 | 0.7
| JPT | 77.9 | 21.2 | 0.9
| YRI | 90.5 | 9.5 | 0.0
| ASW | 78.9 | 19.3 | 1.8
| CHB | 87.6 | 11.7 | 0.7
| CHD | 89.0 | 10.1 | 0.9
| GIH | 81.2 | 18.8 | 0.0
| LWK | 82.7 | 17.3 | 0.0
| MEX | 56.9 | 37.9 | 5.2
| MKK | 70.5 | 26.3 | 3.2
| TSI | 52.0 | 40.2 | 7.8
| HapMapRevision=28
}}{{PMID|20460425|OA=1
}} the rs1411766 locus may be commonly involved in conferring susceptibility to diabetic nephropathy among subjects with type 1 or type 2 diabetes across different ethnic groups.

{{PMID Auto
|PMID=19252134
|Title=Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=19924099
|Title=Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scan.
|OA=1
}}

{{PMID Auto
|PMID=20835900
|Title=Genetics of diabetes complications.
|OA=1
}}

{{PMID Auto
|PMID=21412220
|Title=An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes.
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}