rs6507875
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6507875(C;C) |
| Make rs6507875(C;G) |
| Make rs6507875(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 18 |
| Position | 48922449 |
| Gene | SMAD7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6507875 |
| dbSNP (classic) | rs6507875 |
| ClinGen | rs6507875 |
| ebi | rs6507875 |
| HLI | rs6507875 |
| Exac | rs6507875 |
| Gnomad | rs6507875 |
| Varsome | rs6507875 |
| LitVar | rs6507875 |
| Map | rs6507875 |
| PheGenI | rs6507875 |
| Biobank | rs6507875 |
| 1000 genomes | rs6507875 |
| hgdp | rs6507875 |
| ensembl | rs6507875 |
| geneview | rs6507875 |
| scholar | rs6507875 |
| rs6507875 | |
| pharmgkb | rs6507875 |
| gwascentral | rs6507875 |
| openSNP | rs6507875 |
| 23andMe | rs6507875 |
| SNPshot | rs6507875 |
| SNPdbe | rs6507875 |
| MSV3d | rs6507875 |
| GWAS Ctlg | rs6507875 |
| Max Magnitude | 0 |
[PMID 25375357
] Multiple Functional Risk Variants in a SMAD7 Enhancer Implicate a Colorectal Cancer Risk Haplotype
