rs1456896
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1456896(A;A) |
| Make rs1456896(A;G) |
| Make rs1456896(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 50264865 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1456896 |
| dbSNP (classic) | rs1456896 |
| ClinGen | rs1456896 |
| ebi | rs1456896 |
| HLI | rs1456896 |
| Exac | rs1456896 |
| Gnomad | rs1456896 |
| Varsome | rs1456896 |
| LitVar | rs1456896 |
| Map | rs1456896 |
| PheGenI | rs1456896 |
| Biobank | rs1456896 |
| 1000 genomes | rs1456896 |
| hgdp | rs1456896 |
| ensembl | rs1456896 |
| geneview | rs1456896 |
| scholar | rs1456896 |
| rs1456896 | |
| pharmgkb | rs1456896 |
| gwascentral | rs1456896 |
| openSNP | rs1456896 |
| 23andMe | rs1456896 |
| SNPshot | rs1456896 |
| SNPdbe | rs1456896 |
| MSV3d | rs1456896 |
| GWAS Ctlg | rs1456896 |
| GMAF | 0.4008 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23128233 ]
|
| Trait | Inflammatory bowel disease |
| Title | Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. |
| Risk Allele | T |
| P-val | 7E-15 |
| Odds Ratio | 1.09 [1.055-1.123] |
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463]
|
| Trait | Crohn's disease |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. |
| Risk Allele | T |
| P-val | 1E-8 |
| Odds Ratio | 1.14 [1.09-1.20] |
[PMID 27684961] Association of the IKZF1 5' UTR variant rs1456896 with lupus nephritis in a northern Han Chinese population.
