rs415890
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs415890(C;C) |
| Make rs415890(C;G) |
| Make rs415890(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 166993145 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs415890 |
| dbSNP (classic) | rs415890 |
| ClinGen | rs415890 |
| ebi | rs415890 |
| HLI | rs415890 |
| Exac | rs415890 |
| Gnomad | rs415890 |
| Varsome | rs415890 |
| LitVar | rs415890 |
| Map | rs415890 |
| PheGenI | rs415890 |
| Biobank | rs415890 |
| 1000 genomes | rs415890 |
| hgdp | rs415890 |
| ensembl | rs415890 |
| geneview | rs415890 |
| scholar | rs415890 |
| rs415890 | |
| pharmgkb | rs415890 |
| gwascentral | rs415890 |
| openSNP | rs415890 |
| 23andMe | rs415890 |
| SNPshot | rs415890 |
| SNPdbe | rs415890 |
| MSV3d | rs415890 |
| GWAS Ctlg | rs415890 |
| GMAF | 0.3935 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| 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 | C |
| P-val | 3E-12 |
| Odds Ratio | 1.17 [1.12-1.22] |
