rs9500256
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9500256(A;A) |
| Make rs9500256(A;G) |
| Make rs9500256(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 57982677 |
| Gene | LOC101927293 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9500256 |
| dbSNP (classic) | rs9500256 |
| ClinGen | rs9500256 |
| ebi | rs9500256 |
| HLI | rs9500256 |
| Exac | rs9500256 |
| Gnomad | rs9500256 |
| Varsome | rs9500256 |
| LitVar | rs9500256 |
| Map | rs9500256 |
| PheGenI | rs9500256 |
| Biobank | rs9500256 |
| 1000 genomes | rs9500256 |
| hgdp | rs9500256 |
| ensembl | rs9500256 |
| geneview | rs9500256 |
| scholar | rs9500256 |
| rs9500256 | |
| pharmgkb | rs9500256 |
| gwascentral | rs9500256 |
| openSNP | rs9500256 |
| 23andMe | rs9500256 |
| SNPshot | rs9500256 |
| SNPdbe | rs9500256 |
| MSV3d | rs9500256 |
| GWAS Ctlg | rs9500256 |
| GMAF | 0.4803 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20208534 ]
|
| Trait | Eosinophilic esophagitis (pediatric) |
| Title | Common variants at 5q22 associate with pediatric eosinophilic esophagitis |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 2.04 [1.52-2.70] |
