rs1032757
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs1032757(C;T) |
| Make rs1032757(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 82643499 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1032757 |
| dbSNP (classic) | rs1032757 |
| ClinGen | rs1032757 |
| ebi | rs1032757 |
| HLI | rs1032757 |
| Exac | rs1032757 |
| Gnomad | rs1032757 |
| Varsome | rs1032757 |
| LitVar | rs1032757 |
| Map | rs1032757 |
| PheGenI | rs1032757 |
| Biobank | rs1032757 |
| 1000 genomes | rs1032757 |
| hgdp | rs1032757 |
| ensembl | rs1032757 |
| geneview | rs1032757 |
| scholar | rs1032757 |
| rs1032757 | |
| pharmgkb | rs1032757 |
| gwascentral | rs1032757 |
| openSNP | rs1032757 |
| 23andMe | rs1032757 |
| SNPshot | rs1032757 |
| SNPdbe | rs1032757 |
| MSV3d | rs1032757 |
| GWAS Ctlg | rs1032757 |
| GMAF | 0.1887 |
| 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 | 0.000002 |
| Odds Ratio | 1.96 [1.40-2.74] |
