rs3104964
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3104964(C;C) |
| Make rs3104964(C;T) |
| Make rs3104964(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 95583508 |
| Gene | C8orf37-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3104964 |
| dbSNP (classic) | rs3104964 |
| ClinGen | rs3104964 |
| ebi | rs3104964 |
| HLI | rs3104964 |
| Exac | rs3104964 |
| Gnomad | rs3104964 |
| Varsome | rs3104964 |
| LitVar | rs3104964 |
| Map | rs3104964 |
| PheGenI | rs3104964 |
| Biobank | rs3104964 |
| 1000 genomes | rs3104964 |
| hgdp | rs3104964 |
| ensembl | rs3104964 |
| geneview | rs3104964 |
| scholar | rs3104964 |
| rs3104964 | |
| pharmgkb | rs3104964 |
| gwascentral | rs3104964 |
| openSNP | rs3104964 |
| 23andMe | rs3104964 |
| SNPshot | rs3104964 |
| SNPdbe | rs3104964 |
| MSV3d | rs3104964 |
| GWAS Ctlg | rs3104964 |
| GMAF | 0.438 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23350875 ]
|
| Trait | Colorectal cancer |
| Title | A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. |
| Risk Allele | |
| P-val | 4E-6 |
| Odds Ratio | 1.27 [1.144-1.398] |
