rs4871611
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4871611(A;A) |
| Make rs4871611(A;G) |
| Make rs4871611(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 125525328 |
| Gene | LOC105375746 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4871611 |
| dbSNP (classic) | rs4871611 |
| ClinGen | rs4871611 |
| ebi | rs4871611 |
| HLI | rs4871611 |
| Exac | rs4871611 |
| Gnomad | rs4871611 |
| Varsome | rs4871611 |
| LitVar | rs4871611 |
| Map | rs4871611 |
| PheGenI | rs4871611 |
| Biobank | rs4871611 |
| 1000 genomes | rs4871611 |
| hgdp | rs4871611 |
| ensembl | rs4871611 |
| geneview | rs4871611 |
| scholar | rs4871611 |
| rs4871611 | |
| pharmgkb | rs4871611 |
| gwascentral | rs4871611 |
| openSNP | rs4871611 |
| 23andMe | rs4871611 |
| SNPshot | rs4871611 |
| SNPdbe | rs4871611 |
| MSV3d | rs4871611 |
| GWAS Ctlg | rs4871611 |
| GMAF | 0.4307 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | Crohn's disease |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. |
| Risk Allele | A |
| P-val | 2E-12 |
| Odds Ratio | 1.17 [1.12-1.23] |
