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rs4462560

From SNPedia

Orientationplus
Stabilizedplus
Make rs4462560(C;C)
Make rs4462560(C;G)
Make rs4462560(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position75355623
GeneMAN2C1, MIR631, NEIL1
is asnp
is mentioned by
dbSNPrs4462560
ebirs4462560
HLIrs4462560
Exacrs4462560
Varsomers4462560
Maprs4462560
PheGenIrs4462560
hapmaprs4462560
1000 genomesrs4462560
hgdprs4462560
ensemblrs4462560
gopubmedrs4462560
geneviewrs4462560
scholarrs4462560
googlers4462560
pharmgkbrs4462560
gwascentralrs4462560
openSNPrs4462560
23andMers4462560
23andMe allrs4462560
SNP Nexus

SNPshotrs4462560
SNPdbers4462560
MSV3drs4462560
GWAS Ctlgrs4462560
GMAF0.41
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 24022861] An NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy


[PMID 18594018OA-icon.png] Functional variants of the NEIL1 and NEIL2 genes and risk and progression of squamous cell carcinoma of the oral cavity and oropharynx.


[PMID 26074017] Association between single nucleotide polymorphisms of MUTYH, hOGG1 and NEIL1 genes, and depression