rs4800353
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4800353(A;A) |
| Make rs4800353(A;G) |
| Make rs4800353(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 22074176 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4800353 |
| dbSNP (classic) | rs4800353 |
| ClinGen | rs4800353 |
| ebi | rs4800353 |
| HLI | rs4800353 |
| Exac | rs4800353 |
| Gnomad | rs4800353 |
| Varsome | rs4800353 |
| LitVar | rs4800353 |
| Map | rs4800353 |
| PheGenI | rs4800353 |
| Biobank | rs4800353 |
| 1000 genomes | rs4800353 |
| hgdp | rs4800353 |
| ensembl | rs4800353 |
| geneview | rs4800353 |
| scholar | rs4800353 |
| rs4800353 | |
| pharmgkb | rs4800353 |
| gwascentral | rs4800353 |
| openSNP | rs4800353 |
| 23andMe | rs4800353 |
| SNPshot | rs4800353 |
| SNPdbe | rs4800353 |
| MSV3d | rs4800353 |
| GWAS Ctlg | rs4800353 |
| 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 | T |
| P-val | 3E-7 |
| Odds Ratio | 1.22 [1.14-1.32] |
