rs10995271
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10995271(C;C) |
| Make rs10995271(C;G) |
| Make rs10995271(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 62678726 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10995271 |
| dbSNP (classic) | rs10995271 |
| ClinGen | rs10995271 |
| ebi | rs10995271 |
| HLI | rs10995271 |
| Exac | rs10995271 |
| Gnomad | rs10995271 |
| Varsome | rs10995271 |
| LitVar | rs10995271 |
| Map | rs10995271 |
| PheGenI | rs10995271 |
| Biobank | rs10995271 |
| 1000 genomes | rs10995271 |
| hgdp | rs10995271 |
| ensembl | rs10995271 |
| geneview | rs10995271 |
| scholar | rs10995271 |
| rs10995271 | |
| pharmgkb | rs10995271 |
| gwascentral | rs10995271 |
| openSNP | rs10995271 |
| 23andMe | rs10995271 |
| SNPshot | rs10995271 |
| SNPdbe | rs10995271 |
| MSV3d | rs10995271 |
| GWAS Ctlg | rs10995271 |
| GMAF | 0.3627 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18587394 ]
|
| Trait | Crohn's disease |
| Title | Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease |
| Risk Allele | C |
| P-val | 3.9999999999999998E-20 |
| Odds Ratio | 1.25 [NR] |
[PMID 19915572] Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
[PMID 24365559] Crohn's disease susceptibility variants in Colombian tuberculosis patients
