rs7746082
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7746082(C;C) |
| Make rs7746082(C;G) |
| Make rs7746082(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 105987394 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7746082 |
| dbSNP (classic) | rs7746082 |
| ClinGen | rs7746082 |
| ebi | rs7746082 |
| HLI | rs7746082 |
| Exac | rs7746082 |
| Gnomad | rs7746082 |
| Varsome | rs7746082 |
| LitVar | rs7746082 |
| Map | rs7746082 |
| PheGenI | rs7746082 |
| Biobank | rs7746082 |
| 1000 genomes | rs7746082 |
| hgdp | rs7746082 |
| ensembl | rs7746082 |
| geneview | rs7746082 |
| scholar | rs7746082 |
| rs7746082 | |
| pharmgkb | rs7746082 |
| gwascentral | rs7746082 |
| openSNP | rs7746082 |
| 23andMe | rs7746082 |
| SNPshot | rs7746082 |
| SNPdbe | rs7746082 |
| MSV3d | rs7746082 |
| GWAS Ctlg | rs7746082 |
| GMAF | 0.1345 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs7746082 |
| PubMedID | [PMID 18587394 ]
|
| Condition | Crohn's disease |
| Gene | Unknown |
| Risk Allele | C |
| pValue | 2.00E-010 |
| OR | 1.17 |
| 95% CI | |
DeCode reports that rs7746082 is associated with susceptibility to Crohn's disease. [PMID 18587394]
[PMID 21752155] Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
