rs13106227
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13106227(A;A) |
| Make rs13106227(A;G) |
| Make rs13106227(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 76497528 |
| Gene | SHROOM3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13106227 |
| dbSNP (classic) | rs13106227 |
| ClinGen | rs13106227 |
| ebi | rs13106227 |
| HLI | rs13106227 |
| Exac | rs13106227 |
| Gnomad | rs13106227 |
| Varsome | rs13106227 |
| LitVar | rs13106227 |
| Map | rs13106227 |
| PheGenI | rs13106227 |
| Biobank | rs13106227 |
| 1000 genomes | rs13106227 |
| hgdp | rs13106227 |
| ensembl | rs13106227 |
| geneview | rs13106227 |
| scholar | rs13106227 |
| rs13106227 | |
| pharmgkb | rs13106227 |
| gwascentral | rs13106227 |
| openSNP | rs13106227 |
| 23andMe | rs13106227 |
| SNPshot | rs13106227 |
| SNPdbe | rs13106227 |
| MSV3d | rs13106227 |
| GWAS Ctlg | rs13106227 |
| GMAF | 0.4477 |
| 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 | 0.000004 |
| Odds Ratio | 1.52 [1.20-1.92] |
