rs167769
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs167769(C;C) |
| Make rs167769(C;T) |
| Make rs167769(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 57109992 |
| Gene | STAT6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs167769 |
| dbSNP (classic) | rs167769 |
| ClinGen | rs167769 |
| ebi | rs167769 |
| HLI | rs167769 |
| Exac | rs167769 |
| Gnomad | rs167769 |
| Varsome | rs167769 |
| LitVar | rs167769 |
| Map | rs167769 |
| PheGenI | rs167769 |
| Biobank | rs167769 |
| 1000 genomes | rs167769 |
| hgdp | rs167769 |
| ensembl | rs167769 |
| geneview | rs167769 |
| scholar | rs167769 |
| rs167769 | |
| pharmgkb | rs167769 |
| gwascentral | rs167769 |
| openSNP | rs167769 |
| 23andMe | rs167769 |
| SNPshot | rs167769 |
| SNPdbe | rs167769 |
| MSV3d | rs167769 |
| GWAS Ctlg | rs167769 |
| GMAF | 0.2792 |
| 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 | 1.36 [1.10-1.69] |
[PMID 21762972] The signal transducer and activator of transcription 6 gene (STAT6) increases the propensity of patients with atopic dermatitis toward disseminated viral skin infections
[PMID 17705862] Optimization of candidate-gene SNP-genotyping by flexible oligonucleotide microarrays; analyzing variations in immune regulator genes of hay-fever samples.
[PMID 20046407] An association study of the signal transducer and activator of transcription 6 gene with periodic psychosis.
[PMID 26048407] Association of STAT6 genetic variants with childhood atopic dermatitis in Taiwanese population
