rs1869839
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1869839(A;A) |
| Make rs1869839(A;G) |
| Make rs1869839(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114717488 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1869839 |
| dbSNP (classic) | rs1869839 |
| ClinGen | rs1869839 |
| ebi | rs1869839 |
| HLI | rs1869839 |
| Exac | rs1869839 |
| Gnomad | rs1869839 |
| Varsome | rs1869839 |
| LitVar | rs1869839 |
| Map | rs1869839 |
| PheGenI | rs1869839 |
| Biobank | rs1869839 |
| 1000 genomes | rs1869839 |
| hgdp | rs1869839 |
| ensembl | rs1869839 |
| geneview | rs1869839 |
| scholar | rs1869839 |
| rs1869839 | |
| pharmgkb | rs1869839 |
| gwascentral | rs1869839 |
| openSNP | rs1869839 |
| 23andMe | rs1869839 |
| SNPshot | rs1869839 |
| SNPdbe | rs1869839 |
| MSV3d | rs1869839 |
| GWAS Ctlg | rs1869839 |
| GMAF | 0.2089 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22936669] |
| Trait | Crohn's disease |
| Title | A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. |
| Risk Allele | |
| P-val | 7E-6 |
| Odds Ratio | 1.20 [1.11-1.3] |
