rs6799767
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6799767(G;G) |
| Make rs6799767(G;T) |
| Make rs6799767(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 176312308 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6799767 |
| dbSNP (classic) | rs6799767 |
| ClinGen | rs6799767 |
| ebi | rs6799767 |
| HLI | rs6799767 |
| Exac | rs6799767 |
| Gnomad | rs6799767 |
| Varsome | rs6799767 |
| LitVar | rs6799767 |
| Map | rs6799767 |
| PheGenI | rs6799767 |
| Biobank | rs6799767 |
| 1000 genomes | rs6799767 |
| hgdp | rs6799767 |
| ensembl | rs6799767 |
| geneview | rs6799767 |
| scholar | rs6799767 |
| rs6799767 | |
| pharmgkb | rs6799767 |
| gwascentral | rs6799767 |
| openSNP | rs6799767 |
| 23andMe | rs6799767 |
| SNPshot | rs6799767 |
| SNPdbe | rs6799767 |
| MSV3d | rs6799767 |
| GWAS Ctlg | rs6799767 |
| GMAF | 0.4839 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | |
| P-val | 4E-7 |
| Odds Ratio | 1.49 [1.18-1.85] |
