{{Rsnum
|rsid=7998202
|Gene=C13orf35
|Chromosome=13
|position=112677554
|Orientation=plus
|GMAF=0.1543
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATP11AUN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.8 | 20.4 | 1.9
| HCB | 83.7 | 16.3 | 0.0
| JPT | 84.1 | 15.9 | 0.0
| YRI | 54.5 | 41.8 | 3.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 83.7 | 16.3 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20858683
|Title=Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
|OA=1
}}