rs454886
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs454886(C;C) |
| Make rs454886(C;T) |
| Make rs454886(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 112810420 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs454886 |
| dbSNP (classic) | rs454886 |
| ClinGen | rs454886 |
| ebi | rs454886 |
| HLI | rs454886 |
| Exac | rs454886 |
| Gnomad | rs454886 |
| Varsome | rs454886 |
| LitVar | rs454886 |
| Map | rs454886 |
| PheGenI | rs454886 |
| Biobank | rs454886 |
| 1000 genomes | rs454886 |
| hgdp | rs454886 |
| ensembl | rs454886 |
| geneview | rs454886 |
| scholar | rs454886 |
| rs454886 | |
| pharmgkb | rs454886 |
| gwascentral | rs454886 |
| openSNP | rs454886 |
| 23andMe | rs454886 |
| SNPshot | rs454886 |
| SNPdbe | rs454886 |
| MSV3d | rs454886 |
| GWAS Ctlg | rs454886 |
| GMAF | 0.3655 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18708403
] 798 invasive breast cancer cases and 843 unaffected controls
- rs454886 per allele odds ratio, 1.23; 95% confidence intervals, 1.05-1.43; P(trend) = 0.01
| ClinVar | |
|---|---|
| Risk | rs454886(C;C) |
| Alt | rs454886(C;C) |
| Reference | rs454886(T;T) |
| Significance | Other |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | APC |
| CLNDBN | Familial colorectal cancer |
| Reversed | 1 |
| HGVS | NC_000005.9:g.112146117A>G |
| CLNSRC | ClinVar |
| CLNACC | RCV000074069.1, |
[PMID 27769064] Genetic polymorphisms of Wnt/β-catenin pathway genes are associated with the efficacy and toxicities of radiotherapy in patients with nasopharyngeal carcinoma.
