rs7236477
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common on affy axiom data |
| Make rs7236477(A;G) |
| Make rs7236477(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 31322359 |
| Gene | DSG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7236477 |
| dbSNP (classic) | rs7236477 |
| ClinGen | rs7236477 |
| ebi | rs7236477 |
| HLI | rs7236477 |
| Exac | rs7236477 |
| Gnomad | rs7236477 |
| Varsome | rs7236477 |
| LitVar | rs7236477 |
| Map | rs7236477 |
| PheGenI | rs7236477 |
| Biobank | rs7236477 |
| 1000 genomes | rs7236477 |
| hgdp | rs7236477 |
| ensembl | rs7236477 |
| geneview | rs7236477 |
| scholar | rs7236477 |
| rs7236477 | |
| pharmgkb | rs7236477 |
| gwascentral | rs7236477 |
| openSNP | rs7236477 |
| 23andMe | rs7236477 |
| SNPshot | rs7236477 |
| SNPdbe | rs7236477 |
| MSV3d | rs7236477 |
| GWAS Ctlg | rs7236477 |
| GMAF | 0.06382 |
| 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 | G |
| P-val | 0.000007 |
| Odds Ratio | 2.22 [1.39-3.55] |
