{{Rsnum
|rsid=4462560
|Gene=MAN2C1
|Chromosome=15
|position=75355623
|Orientation=plus
|GMAF=0.41
|Gene_s=MAN2C1,MIR631,NEIL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 65.1 | 30.2 | 4.8
| HCB | 26.7 | 55.6 | 17.8
| JPT | 22.7 | 56.8 | 20.5
| YRI | 16.1 | 48.4 | 35.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.7 | 55.6 | 17.8
| 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=24022861
|Title=An NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy
}}

{{PMID Auto
|PMID=18594018
|Title=Functional variants of the NEIL1 and NEIL2 genes and risk and progression of squamous cell carcinoma of the oral cavity and oropharynx.
|OA=1
}}

{{on chip | HumanOmni1Quad}}