rs10904849
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10904849(G;T) |
| Make rs10904849(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 16955267 |
| Gene | CUBN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10904849 |
| dbSNP (classic) | rs10904849 |
| ClinGen | rs10904849 |
| ebi | rs10904849 |
| HLI | rs10904849 |
| Exac | rs10904849 |
| Gnomad | rs10904849 |
| Varsome | rs10904849 |
| LitVar | rs10904849 |
| Map | rs10904849 |
| PheGenI | rs10904849 |
| Biobank | rs10904849 |
| 1000 genomes | rs10904849 |
| hgdp | rs10904849 |
| ensembl | rs10904849 |
| geneview | rs10904849 |
| scholar | rs10904849 |
| rs10904849 | |
| pharmgkb | rs10904849 |
| gwascentral | rs10904849 |
| openSNP | rs10904849 |
| 23andMe | rs10904849 |
| SNPshot | rs10904849 |
| SNPdbe | rs10904849 |
| MSV3d | rs10904849 |
| GWAS Ctlg | rs10904849 |
| Max Magnitude | 0 |
[PMID 29403313
] Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score
