rs1456893
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1456893(A;A) |
| Make rs1456893(A;G) |
| Make rs1456893(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 50230076 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1456893 |
| dbSNP (classic) | rs1456893 |
| ClinGen | rs1456893 |
| ebi | rs1456893 |
| HLI | rs1456893 |
| Exac | rs1456893 |
| Gnomad | rs1456893 |
| Varsome | rs1456893 |
| LitVar | rs1456893 |
| Map | rs1456893 |
| PheGenI | rs1456893 |
| Biobank | rs1456893 |
| 1000 genomes | rs1456893 |
| hgdp | rs1456893 |
| ensembl | rs1456893 |
| geneview | rs1456893 |
| scholar | rs1456893 |
| rs1456893 | |
| pharmgkb | rs1456893 |
| gwascentral | rs1456893 |
| openSNP | rs1456893 |
| 23andMe | rs1456893 |
| SNPshot | rs1456893 |
| SNPdbe | rs1456893 |
| MSV3d | rs1456893 |
| GWAS Ctlg | rs1456893 |
| GMAF | 0.3857 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | A |
| P-val | 5.0000000000000001E-9 |
| Odds Ratio | 1.20 [NR] |
DeCode reports that rs1456893 is associated with susceptibility to Crohn's disease. [PMID 18587394]
[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 21830272] Distinct and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlations with pathogenesis.
