{{Rsnum
|rsid=293795
|Gene=OGG1
|Chromosome=3
|position=9757429
|Orientation=minus
|GMAF=0.1616
|Gene_s=CAMK1,OGG1
|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 | 0.9 | 25.9 | 73.2
| HCB | 0.7 | 8.0 | 91.2
| JPT | 0.0 | 7.1 | 92.9
| YRI | 9.6 | 47.3 | 43.2
| ASW | 8.8 | 49.1 | 42.1
| CHB | 0.7 | 8.0 | 91.2
| CHD | 0.0 | 5.5 | 94.5
| GIH | 0.0 | 15.8 | 84.2
| LWK | 11.1 | 45.4 | 43.5
| MEX | 3.5 | 19.3 | 77.2
| MKK | 4.5 | 34.2 | 61.3
| TSI | 2.0 | 18.6 | 79.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22389292
|Title=An exploratory case-only analysis of gene-hazardous air pollutant interactions and the risk of childhood medulloblastoma
|OA=1
}}

{{PMID Auto
|PMID=24022861
|Title=An NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy
}}

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