rs4462560
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4462560(C;C) |
| Make rs4462560(C;G) |
| Make rs4462560(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 75355623 |
| Gene | MAN2C1, MIR631, NEIL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4462560 |
| dbSNP (classic) | rs4462560 |
| ClinGen | rs4462560 |
| ebi | rs4462560 |
| HLI | rs4462560 |
| Exac | rs4462560 |
| Gnomad | rs4462560 |
| Varsome | rs4462560 |
| LitVar | rs4462560 |
| Map | rs4462560 |
| PheGenI | rs4462560 |
| Biobank | rs4462560 |
| 1000 genomes | rs4462560 |
| hgdp | rs4462560 |
| ensembl | rs4462560 |
| geneview | rs4462560 |
| scholar | rs4462560 |
| rs4462560 | |
| pharmgkb | rs4462560 |
| gwascentral | rs4462560 |
| openSNP | rs4462560 |
| 23andMe | rs4462560 |
| SNPshot | rs4462560 |
| SNPdbe | rs4462560 |
| MSV3d | rs4462560 |
| GWAS Ctlg | rs4462560 |
| GMAF | 0.41 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 24022861] An NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy
[PMID 18594018
] 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
