rs200403177
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs200403177(A;A) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 132673598 |
| Gene | POLE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200403177 |
| dbSNP (classic) | rs200403177 |
| ClinGen | rs200403177 |
| ebi | rs200403177 |
| HLI | rs200403177 |
| Exac | rs200403177 |
| Gnomad | rs200403177 |
| Varsome | rs200403177 |
| LitVar | rs200403177 |
| Map | rs200403177 |
| PheGenI | rs200403177 |
| Biobank | rs200403177 |
| 1000 genomes | rs200403177 |
| hgdp | rs200403177 |
| ensembl | rs200403177 |
| geneview | rs200403177 |
| scholar | rs200403177 |
| rs200403177 | |
| pharmgkb | rs200403177 |
| gwascentral | rs200403177 |
| openSNP | rs200403177 |
| 23andMe | rs200403177 |
| SNPshot | rs200403177 |
| SNPdbe | rs200403177 |
| MSV3d | rs200403177 |
| GWAS Ctlg | rs200403177 |
| Max Magnitude | 0 |
aka c.1336C>T, p.Arg446Trp
Heterozygotes are predicted to have a significantly higher risk of colorectal cancer, based on both patient and theoretical studies.[PMID 23263490
]
