rs11167764
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11167764(A;A) |
| Make rs11167764(A;C) |
| Make rs11167764(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 142099500 |
| Gene | LOC105378204 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11167764 |
| dbSNP (classic) | rs11167764 |
| ClinGen | rs11167764 |
| ebi | rs11167764 |
| HLI | rs11167764 |
| Exac | rs11167764 |
| Gnomad | rs11167764 |
| Varsome | rs11167764 |
| LitVar | rs11167764 |
| Map | rs11167764 |
| PheGenI | rs11167764 |
| Biobank | rs11167764 |
| 1000 genomes | rs11167764 |
| hgdp | rs11167764 |
| ensembl | rs11167764 |
| geneview | rs11167764 |
| scholar | rs11167764 |
| rs11167764 | |
| pharmgkb | rs11167764 |
| gwascentral | rs11167764 |
| openSNP | rs11167764 |
| 23andMe | rs11167764 |
| SNPshot | rs11167764 |
| SNPdbe | rs11167764 |
| MSV3d | rs11167764 |
| GWAS Ctlg | rs11167764 |
| GMAF | 0.2025 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | C |
| P-val | 2E-9 |
| Odds Ratio | 1.0600 [1.02-1.11] |
