rs3094188
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3094188(G;G) |
| Make rs3094188(G;T) |
| Make rs3094188(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31174468 |
| Gene | PSORS1C3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3094188 |
| dbSNP (classic) | rs3094188 |
| ClinGen | rs3094188 |
| ebi | rs3094188 |
| HLI | rs3094188 |
| Exac | rs3094188 |
| Gnomad | rs3094188 |
| Varsome | rs3094188 |
| LitVar | rs3094188 |
| Map | rs3094188 |
| PheGenI | rs3094188 |
| Biobank | rs3094188 |
| 1000 genomes | rs3094188 |
| hgdp | rs3094188 |
| ensembl | rs3094188 |
| geneview | rs3094188 |
| scholar | rs3094188 |
| rs3094188 | |
| pharmgkb | rs3094188 |
| gwascentral | rs3094188 |
| openSNP | rs3094188 |
| 23andMe | rs3094188 |
| SNPshot | rs3094188 |
| SNPdbe | rs3094188 |
| MSV3d | rs3094188 |
| GWAS Ctlg | rs3094188 |
| GMAF | 0.281 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23266558] |
| Trait | Crohn's disease |
| Title | A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population. |
| Risk Allele | C |
| P-val | 7E-7 |
| Odds Ratio | 1.61 [1.33-1.94] |
[PMID 26049586] A human leukocyte antigen locus haplotype confers risk for allopurinol-related adverse effects in Caucasian patients with gout
