rs2274910
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2274910(C;C) |
| Make rs2274910(C;T) |
| Make rs2274910(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 160882256 |
| Gene | ITLN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2274910 |
| dbSNP (classic) | rs2274910 |
| ClinGen | rs2274910 |
| ebi | rs2274910 |
| HLI | rs2274910 |
| Exac | rs2274910 |
| Gnomad | rs2274910 |
| Varsome | rs2274910 |
| LitVar | rs2274910 |
| Map | rs2274910 |
| PheGenI | rs2274910 |
| Biobank | rs2274910 |
| 1000 genomes | rs2274910 |
| hgdp | rs2274910 |
| ensembl | rs2274910 |
| geneview | rs2274910 |
| scholar | rs2274910 |
| rs2274910 | |
| pharmgkb | rs2274910 |
| gwascentral | rs2274910 |
| openSNP | rs2274910 |
| 23andMe | rs2274910 |
| SNPshot | rs2274910 |
| SNPdbe | rs2274910 |
| MSV3d | rs2274910 |
| GWAS Ctlg | rs2274910 |
| GMAF | 0.3976 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 1.0000000000000001E-9 |
| Odds Ratio | 1.14 [NR] |
[PMID 19068216] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
[PMID 22573572] Phenotype-genotype profiles in Crohn's disease predicted by genetic markers in autophagy-related genes (GOIA study II).
