rs1799798
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1799798(A;A) |
| Make rs1799798(A;G) |
| Make rs1799798(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 13920421 |
| Gene | ERCC4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1799798 |
| dbSNP (classic) | rs1799798 |
| ClinGen | rs1799798 |
| ebi | rs1799798 |
| HLI | rs1799798 |
| Exac | rs1799798 |
| Gnomad | rs1799798 |
| Varsome | rs1799798 |
| LitVar | rs1799798 |
| Map | rs1799798 |
| PheGenI | rs1799798 |
| Biobank | rs1799798 |
| 1000 genomes | rs1799798 |
| hgdp | rs1799798 |
| ensembl | rs1799798 |
| geneview | rs1799798 |
| scholar | rs1799798 |
| rs1799798 | |
| pharmgkb | rs1799798 |
| gwascentral | rs1799798 |
| openSNP | rs1799798 |
| 23andMe | rs1799798 |
| SNPshot | rs1799798 |
| SNPdbe | rs1799798 |
| MSV3d | rs1799798 |
| GWAS Ctlg | rs1799798 |
| Max Magnitude | 0 |
[PMID 24938470] Association of polymorphisms of the xeroderma pigmentosum complementation group F gene with increased glioma risk
