rs4911642
From SNPedia
| Orientation | minus |
| Stabilized | plus |
| Make rs4911642(C;C) |
| Make rs4911642(C;T) |
| Make rs4911642(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 15473564 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4911642 |
| dbSNP (classic) | rs4911642 |
| ClinGen | rs4911642 |
| ebi | rs4911642 |
| HLI | rs4911642 |
| Exac | rs4911642 |
| Gnomad | rs4911642 |
| Varsome | rs4911642 |
| LitVar | rs4911642 |
| Map | rs4911642 |
| PheGenI | rs4911642 |
| Biobank | rs4911642 |
| 1000 genomes | rs4911642 |
| hgdp | rs4911642 |
| ensembl | rs4911642 |
| geneview | rs4911642 |
| scholar | rs4911642 |
| rs4911642 | |
| pharmgkb | rs4911642 |
| gwascentral | rs4911642 |
| openSNP | rs4911642 |
| 23andMe | rs4911642 |
| SNPshot | rs4911642 |
| SNPdbe | rs4911642 |
| MSV3d | rs4911642 |
| GWAS Ctlg | rs4911642 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 23936387 ]
|
| Trait | Celiac disease |
| Title | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
| Risk Allele | C |
| P-val | 5E-6 |
| Odds Ratio | NR NR |
