rs1487630
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1487630(A;A) |
| Make rs1487630(A;G) |
| Make rs1487630(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 38334202 |
| Gene | LOC105374410 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1487630 |
| dbSNP (classic) | rs1487630 |
| ClinGen | rs1487630 |
| ebi | rs1487630 |
| HLI | rs1487630 |
| Exac | rs1487630 |
| Gnomad | rs1487630 |
| Varsome | rs1487630 |
| LitVar | rs1487630 |
| Map | rs1487630 |
| PheGenI | rs1487630 |
| Biobank | rs1487630 |
| 1000 genomes | rs1487630 |
| hgdp | rs1487630 |
| ensembl | rs1487630 |
| geneview | rs1487630 |
| scholar | rs1487630 |
| rs1487630 | |
| pharmgkb | rs1487630 |
| gwascentral | rs1487630 |
| openSNP | rs1487630 |
| 23andMe | rs1487630 |
| SNPshot | rs1487630 |
| SNPdbe | rs1487630 |
| MSV3d | rs1487630 |
| GWAS Ctlg | rs1487630 |
| GMAF | 0.1726 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23266558] |
| Trait | Crohn's disease |
| Title | A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population. |
| Risk Allele | T |
| P-val | 1E-11 |
| Odds Ratio | 1.33 [1.22-1.44] |
