rs167715
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs167715(C;C) |
| Make rs167715(C;T) |
| Make rs167715(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 103977589 |
| Gene | TDG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs167715 |
| dbSNP (classic) | rs167715 |
| ClinGen | rs167715 |
| ebi | rs167715 |
| HLI | rs167715 |
| Exac | rs167715 |
| Gnomad | rs167715 |
| Varsome | rs167715 |
| LitVar | rs167715 |
| Map | rs167715 |
| PheGenI | rs167715 |
| Biobank | rs167715 |
| 1000 genomes | rs167715 |
| hgdp | rs167715 |
| ensembl | rs167715 |
| geneview | rs167715 |
| scholar | rs167715 |
| rs167715 | |
| pharmgkb | rs167715 |
| gwascentral | rs167715 |
| openSNP | rs167715 |
| 23andMe | rs167715 |
| SNPshot | rs167715 |
| SNPdbe | rs167715 |
| MSV3d | rs167715 |
| GWAS Ctlg | rs167715 |
| GMAF | 0.07346 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 20226869
] Association between genetic variants in the base excision repair pathway and outcomes after hematopoietic cell transplants
