rs181359
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs181359(C;C) |
| Make rs181359(C;T) |
| Make rs181359(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 22 |
| Position | 21574352 |
| Gene | UBE2L3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs181359 |
| dbSNP (classic) | rs181359 |
| ClinGen | rs181359 |
| ebi | rs181359 |
| HLI | rs181359 |
| Exac | rs181359 |
| Gnomad | rs181359 |
| Varsome | rs181359 |
| LitVar | rs181359 |
| Map | rs181359 |
| PheGenI | rs181359 |
| Biobank | rs181359 |
| 1000 genomes | rs181359 |
| hgdp | rs181359 |
| ensembl | rs181359 |
| geneview | rs181359 |
| scholar | rs181359 |
| rs181359 | |
| pharmgkb | rs181359 |
| gwascentral | rs181359 |
| openSNP | rs181359 |
| 23andMe | rs181359 |
| SNPshot | rs181359 |
| SNPdbe | rs181359 |
| MSV3d | rs181359 |
| GWAS Ctlg | rs181359 |
| GMAF | 0.2759 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
| Risk Allele | T |
| P-val | 5E-16 |
| Odds Ratio | 1.1000 [1.06-1.15] |
[PMID 22482804] Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci
