rs2178146
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2178146(A;A) |
| Make rs2178146(A;G) |
| Make rs2178146(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 86430089 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2178146 |
| dbSNP (classic) | rs2178146 |
| ClinGen | rs2178146 |
| ebi | rs2178146 |
| HLI | rs2178146 |
| Exac | rs2178146 |
| Gnomad | rs2178146 |
| Varsome | rs2178146 |
| LitVar | rs2178146 |
| Map | rs2178146 |
| PheGenI | rs2178146 |
| Biobank | rs2178146 |
| 1000 genomes | rs2178146 |
| hgdp | rs2178146 |
| ensembl | rs2178146 |
| geneview | rs2178146 |
| scholar | rs2178146 |
| rs2178146 | |
| pharmgkb | rs2178146 |
| gwascentral | rs2178146 |
| openSNP | rs2178146 |
| 23andMe | rs2178146 |
| SNPshot | rs2178146 |
| SNPdbe | rs2178146 |
| MSV3d | rs2178146 |
| GWAS Ctlg | rs2178146 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24121790 ]
|
| Trait | Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) |
| Title | A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. |
| Risk Allele | A |
| P-val | 1E-6 |
| Odds Ratio | 1.14 [1.09-1.2] |
