rs207906
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs207906(A;A) |
| Make rs207906(A;G) |
| Make rs207906(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 216148178 |
| Gene | XRCC5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs207906 |
| dbSNP (classic) | rs207906 |
| ClinGen | rs207906 |
| ebi | rs207906 |
| HLI | rs207906 |
| Exac | rs207906 |
| Gnomad | rs207906 |
| Varsome | rs207906 |
| LitVar | rs207906 |
| Map | rs207906 |
| PheGenI | rs207906 |
| Biobank | rs207906 |
| 1000 genomes | rs207906 |
| hgdp | rs207906 |
| ensembl | rs207906 |
| geneview | rs207906 |
| scholar | rs207906 |
| rs207906 | |
| pharmgkb | rs207906 |
| gwascentral | rs207906 |
| openSNP | rs207906 |
| 23andMe | rs207906 |
| SNPshot | rs207906 |
| SNPdbe | rs207906 |
| MSV3d | rs207906 |
| GWAS Ctlg | rs207906 |
| GMAF | 0.1065 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21346221] Risk of acute promyelocytic leukemia in multiple sclerosis: Coding variants of DNA repair genes
[PMID 24615081] Association of XRCC5 polymorphisms with COPD and COPD-related phenotypes in the Han Chinese population: a case-control cohort study.
