rs2074404
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2074404(G;G) |
| Make rs2074404(G;T) |
| Make rs2074404(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 46788073 |
| Gene | WNT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2074404 |
| dbSNP (classic) | rs2074404 |
| ClinGen | rs2074404 |
| ebi | rs2074404 |
| HLI | rs2074404 |
| Exac | rs2074404 |
| Gnomad | rs2074404 |
| Varsome | rs2074404 |
| LitVar | rs2074404 |
| Map | rs2074404 |
| PheGenI | rs2074404 |
| Biobank | rs2074404 |
| 1000 genomes | rs2074404 |
| hgdp | rs2074404 |
| ensembl | rs2074404 |
| geneview | rs2074404 |
| scholar | rs2074404 |
| rs2074404 | |
| pharmgkb | rs2074404 |
| gwascentral | rs2074404 |
| openSNP | rs2074404 |
| 23andMe | rs2074404 |
| SNPshot | rs2074404 |
| SNPdbe | rs2074404 |
| MSV3d | rs2074404 |
| GWAS Ctlg | rs2074404 |
| GMAF | 0.348 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 ]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | 1.11 [1.06-1.16] |
[PMID 24871462] Coeliac disease-associated polymorphisms influence thymic gene expression
