rs13278732
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13278732(C;C) |
| Make rs13278732(C;T) |
| Make rs13278732(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 98076353 |
| Gene | ERICH5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13278732 |
| dbSNP (classic) | rs13278732 |
| ClinGen | rs13278732 |
| ebi | rs13278732 |
| HLI | rs13278732 |
| Exac | rs13278732 |
| Gnomad | rs13278732 |
| Varsome | rs13278732 |
| LitVar | rs13278732 |
| Map | rs13278732 |
| PheGenI | rs13278732 |
| Biobank | rs13278732 |
| 1000 genomes | rs13278732 |
| hgdp | rs13278732 |
| ensembl | rs13278732 |
| geneview | rs13278732 |
| scholar | rs13278732 |
| rs13278732 | |
| pharmgkb | rs13278732 |
| gwascentral | rs13278732 |
| openSNP | rs13278732 |
| 23andMe | rs13278732 |
| SNPshot | rs13278732 |
| SNPdbe | rs13278732 |
| MSV3d | rs13278732 |
| GWAS Ctlg | rs13278732 |
| GMAF | 0.1722 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | T |
| P-val | 0.000006 |
| Odds Ratio | 1.31 [1.04-1.65] |
