rs1998598
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1998598(A;A) |
| Make rs1998598(A;G) |
| Make rs1998598(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 197758512 |
| Gene | DENND1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1998598 |
| dbSNP (classic) | rs1998598 |
| ClinGen | rs1998598 |
| ebi | rs1998598 |
| HLI | rs1998598 |
| Exac | rs1998598 |
| Gnomad | rs1998598 |
| Varsome | rs1998598 |
| LitVar | rs1998598 |
| Map | rs1998598 |
| PheGenI | rs1998598 |
| Biobank | rs1998598 |
| 1000 genomes | rs1998598 |
| hgdp | rs1998598 |
| ensembl | rs1998598 |
| geneview | rs1998598 |
| scholar | rs1998598 |
| rs1998598 | |
| pharmgkb | rs1998598 |
| gwascentral | rs1998598 |
| openSNP | rs1998598 |
| 23andMe | rs1998598 |
| SNPshot | rs1998598 |
| SNPdbe | rs1998598 |
| MSV3d | rs1998598 |
| GWAS Ctlg | rs1998598 |
| GMAF | 0.225 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
| Risk Allele | G |
| P-val | 9E-9 |
| Odds Ratio | 1.0400 [1.00-1.09] |
