rs1373692
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1373692(G;G) |
| Make rs1373692(G;T) |
| Make rs1373692(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 40431081 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1373692 |
| dbSNP (classic) | rs1373692 |
| ClinGen | rs1373692 |
| ebi | rs1373692 |
| HLI | rs1373692 |
| Exac | rs1373692 |
| Gnomad | rs1373692 |
| Varsome | rs1373692 |
| LitVar | rs1373692 |
| Map | rs1373692 |
| PheGenI | rs1373692 |
| Biobank | rs1373692 |
| 1000 genomes | rs1373692 |
| hgdp | rs1373692 |
| ensembl | rs1373692 |
| geneview | rs1373692 |
| scholar | rs1373692 |
| rs1373692 | |
| pharmgkb | rs1373692 |
| gwascentral | rs1373692 |
| openSNP | rs1373692 |
| 23andMe | rs1373692 |
| SNPshot | rs1373692 |
| SNPdbe | rs1373692 |
| MSV3d | rs1373692 |
| GWAS Ctlg | rs1373692 |
| GMAF | 0.4761 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs1373692 increases susceptibility to Crohn's disease 1.46 times for carriers of the G allele [PMID 17447842
]
| GWAS | |
|---|---|
| SNP | rs1373692 |
| PubMedID | [PMID 17447842]
|
| Condition | Crohn's disease |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 2.00E-012 |
| OR | 1.46 |
| 95% CI | |
