rs1799787
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1799787(C;C) |
| Make rs1799787(C;T) |
| Make rs1799787(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 45352886 |
| Gene | ERCC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799787 |
| dbSNP (classic) | rs1799787 |
| ClinGen | rs1799787 |
| ebi | rs1799787 |
| HLI | rs1799787 |
| Exac | rs1799787 |
| Gnomad | rs1799787 |
| Varsome | rs1799787 |
| LitVar | rs1799787 |
| Map | rs1799787 |
| PheGenI | rs1799787 |
| Biobank | rs1799787 |
| 1000 genomes | rs1799787 |
| hgdp | rs1799787 |
| ensembl | rs1799787 |
| geneview | rs1799787 |
| scholar | rs1799787 |
| rs1799787 | |
| pharmgkb | rs1799787 |
| gwascentral | rs1799787 |
| openSNP | rs1799787 |
| 23andMe | rs1799787 |
| SNPshot | rs1799787 |
| SNPdbe | rs1799787 |
| MSV3d | rs1799787 |
| GWAS Ctlg | rs1799787 |
| GMAF | 0.1823 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 19406934] HapMap-based study of the DNA repair gene ERCC2 and lung cancer susceptibility in a Chinese population
[PMID 22351191] Hapmap-based evaluation of ERCC2, PPP1R13L, and ERCC1 and lung cancer risk in a Chinese population
[PMID 16026601
] Decision forest analysis of 61 single nucleotide polymorphisms in a case-control study of esophageal cancer; a novel method.
[PMID 18709642] Nucleotide excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African Americans.
