rs2224865
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2224865(G;G) |
| Make rs2224865(G;T) |
| Make rs2224865(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 83663098 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2224865 |
| dbSNP (classic) | rs2224865 |
| ClinGen | rs2224865 |
| ebi | rs2224865 |
| HLI | rs2224865 |
| Exac | rs2224865 |
| Gnomad | rs2224865 |
| Varsome | rs2224865 |
| LitVar | rs2224865 |
| Map | rs2224865 |
| PheGenI | rs2224865 |
| Biobank | rs2224865 |
| 1000 genomes | rs2224865 |
| hgdp | rs2224865 |
| ensembl | rs2224865 |
| geneview | rs2224865 |
| scholar | rs2224865 |
| rs2224865 | |
| pharmgkb | rs2224865 |
| gwascentral | rs2224865 |
| openSNP | rs2224865 |
| 23andMe | rs2224865 |
| SNPshot | rs2224865 |
| SNPdbe | rs2224865 |
| MSV3d | rs2224865 |
| GWAS Ctlg | rs2224865 |
| GMAF | 0.3531 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20208534 ]
|
| Trait | Eosinophilic esophagitis (pediatric) |
| Title | Common variants at 5q22 associate with pediatric eosinophilic esophagitis |
| Risk Allele | G |
| P-val | 0.000009 |
| Odds Ratio | 1.44 [1.15-1.79] |
