rs3806932
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3806932(A;A) |
| Make rs3806932(A;G) |
| Make rs3806932(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 111069977 |
| Gene | TSLP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3806932 |
| dbSNP (classic) | rs3806932 |
| ClinGen | rs3806932 |
| ebi | rs3806932 |
| HLI | rs3806932 |
| Exac | rs3806932 |
| Gnomad | rs3806932 |
| Varsome | rs3806932 |
| LitVar | rs3806932 |
| Map | rs3806932 |
| PheGenI | rs3806932 |
| Biobank | rs3806932 |
| 1000 genomes | rs3806932 |
| hgdp | rs3806932 |
| ensembl | rs3806932 |
| geneview | rs3806932 |
| scholar | rs3806932 |
| rs3806932 | |
| pharmgkb | rs3806932 |
| gwascentral | rs3806932 |
| openSNP | rs3806932 |
| 23andMe | rs3806932 |
| SNPshot | rs3806932 |
| SNPdbe | rs3806932 |
| MSV3d | rs3806932 |
| GWAS Ctlg | rs3806932 |
| GMAF | 0.4692 |
| 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 | 3E-9 |
| Odds Ratio | 1.85 None |
