rs740495
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs740495(C;C) |
| Make rs740495(C;T) |
| Make rs740495(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 1124836 |
| Gene | SBNO2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs740495 |
| dbSNP (classic) | rs740495 |
| ClinGen | rs740495 |
| ebi | rs740495 |
| HLI | rs740495 |
| Exac | rs740495 |
| Gnomad | rs740495 |
| Varsome | rs740495 |
| LitVar | rs740495 |
| Map | rs740495 |
| PheGenI | rs740495 |
| Biobank | rs740495 |
| 1000 genomes | rs740495 |
| hgdp | rs740495 |
| ensembl | rs740495 |
| geneview | rs740495 |
| scholar | rs740495 |
| rs740495 | |
| pharmgkb | rs740495 |
| gwascentral | rs740495 |
| openSNP | rs740495 |
| 23andMe | rs740495 |
| SNPshot | rs740495 |
| SNPdbe | rs740495 |
| MSV3d | rs740495 |
| GWAS Ctlg | rs740495 |
| GMAF | 0.3852 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | G |
| P-val | 8E-12 |
| Odds Ratio | 1.16 [1.10-1.21] |
