rs371915
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs371915(A;A) |
| Make rs371915(A;G) |
| Make rs371915(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 84544635 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371915 |
| dbSNP (classic) | rs371915 |
| ClinGen | rs371915 |
| ebi | rs371915 |
| HLI | rs371915 |
| Exac | rs371915 |
| Gnomad | rs371915 |
| Varsome | rs371915 |
| LitVar | rs371915 |
| Map | rs371915 |
| PheGenI | rs371915 |
| Biobank | rs371915 |
| 1000 genomes | rs371915 |
| hgdp | rs371915 |
| ensembl | rs371915 |
| geneview | rs371915 |
| scholar | rs371915 |
| rs371915 | |
| pharmgkb | rs371915 |
| gwascentral | rs371915 |
| openSNP | rs371915 |
| 23andMe | rs371915 |
| SNPshot | rs371915 |
| SNPdbe | rs371915 |
| MSV3d | rs371915 |
| GWAS Ctlg | rs371915 |
| GMAF | 0.1405 |
| 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 | 2E-8 |
| Odds Ratio | 1.90 [1.44-2.50] |
