rs3787089
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3787089(A;A) |
| Make rs3787089(A;G) |
| Make rs3787089(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 20 |
| Position | 63685277 |
| Gene | RTEL1, RTEL1-TNFRSF6B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3787089 |
| dbSNP (classic) | rs3787089 |
| ClinGen | rs3787089 |
| ebi | rs3787089 |
| HLI | rs3787089 |
| Exac | rs3787089 |
| Gnomad | rs3787089 |
| Varsome | rs3787089 |
| LitVar | rs3787089 |
| Map | rs3787089 |
| PheGenI | rs3787089 |
| Biobank | rs3787089 |
| 1000 genomes | rs3787089 |
| hgdp | rs3787089 |
| ensembl | rs3787089 |
| geneview | rs3787089 |
| scholar | rs3787089 |
| rs3787089 | |
| pharmgkb | rs3787089 |
| gwascentral | rs3787089 |
| openSNP | rs3787089 |
| 23andMe | rs3787089 |
| SNPshot | rs3787089 |
| SNPdbe | rs3787089 |
| MSV3d | rs3787089 |
| GWAS Ctlg | rs3787089 |
| Max Magnitude | 0 |
[PMID 30462709
] Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population.
