rs891835
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | ||
| (T;T) | 0 |
| Make rs891835(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 129479506 |
| Gene | CCDC26 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs891835 |
| dbSNP (classic) | rs891835 |
| ClinGen | rs891835 |
| ebi | rs891835 |
| HLI | rs891835 |
| Exac | rs891835 |
| Gnomad | rs891835 |
| Varsome | rs891835 |
| LitVar | rs891835 |
| Map | rs891835 |
| PheGenI | rs891835 |
| Biobank | rs891835 |
| 1000 genomes | rs891835 |
| hgdp | rs891835 |
| ensembl | rs891835 |
| geneview | rs891835 |
| scholar | rs891835 |
| rs891835 | |
| pharmgkb | rs891835 |
| gwascentral | rs891835 |
| openSNP | rs891835 |
| 23andMe | rs891835 |
| SNPshot | rs891835 |
| SNPdbe | rs891835 |
| MSV3d | rs891835 |
| GWAS Ctlg | rs891835 |
| GMAF | 0.1593 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19578367 ]
|
| Trait | Glioma |
| Title | Genome-wide association study identifies five susceptibility loci for glioma |
| Risk Allele | G |
| P-val | 8E-11 |
| Odds Ratio | 1.24 [1.17-1.30] |
[PMID 20368557] Polymorphisms of LIG4, BTBD2, HMGA2, and RTEL1 genes involved in the double-strand break repair pathway predict glioblastoma survival.
[PMID 24870769] CCDC26 Gene Polymorphism and Glioblastoma Risk in the Han Chinese Population
[PMID 26014354] CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility
