rs50872
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs50872(C;C) |
| Make rs50872(C;T) |
| Make rs50872(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 45359191 |
| Gene | ERCC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs50872 |
| dbSNP (classic) | rs50872 |
| ClinGen | rs50872 |
| ebi | rs50872 |
| HLI | rs50872 |
| Exac | rs50872 |
| Gnomad | rs50872 |
| Varsome | rs50872 |
| LitVar | rs50872 |
| Map | rs50872 |
| PheGenI | rs50872 |
| Biobank | rs50872 |
| 1000 genomes | rs50872 |
| hgdp | rs50872 |
| ensembl | rs50872 |
| geneview | rs50872 |
| scholar | rs50872 |
| rs50872 | |
| pharmgkb | rs50872 |
| gwascentral | rs50872 |
| openSNP | rs50872 |
| 23andMe | rs50872 |
| SNPshot | rs50872 |
| SNPdbe | rs50872 |
| MSV3d | rs50872 |
| GWAS Ctlg | rs50872 |
| GMAF | 0.208 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21751184] SNP-SNP interactions between DNA repair genes were associated with breast cancer risk in a Korean population
[PMID 20128036
] DNA polymorphism and risk of esophageal squamous cell carcinoma in a population of North Xinjiang, China.
[PMID 22608006] Clinical significance of ERCC2 haplotype-tagging single nucleotide polymorphisms in patients with unresectable non-small cell lung cancer treated with first-line platinum-based chemotherapy
