rs4902642
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4902642(A;A) |
| Make rs4902642(A;G) |
| Make rs4902642(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 68743482 |
| Gene | LOC107984647 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4902642 |
| dbSNP (classic) | rs4902642 |
| ClinGen | rs4902642 |
| ebi | rs4902642 |
| HLI | rs4902642 |
| Exac | rs4902642 |
| Gnomad | rs4902642 |
| Varsome | rs4902642 |
| LitVar | rs4902642 |
| Map | rs4902642 |
| PheGenI | rs4902642 |
| Biobank | rs4902642 |
| 1000 genomes | rs4902642 |
| hgdp | rs4902642 |
| ensembl | rs4902642 |
| geneview | rs4902642 |
| scholar | rs4902642 |
| rs4902642 | |
| pharmgkb | rs4902642 |
| gwascentral | rs4902642 |
| openSNP | rs4902642 |
| 23andMe | rs4902642 |
| SNPshot | rs4902642 |
| SNPdbe | rs4902642 |
| MSV3d | rs4902642 |
| GWAS Ctlg | rs4902642 |
| GMAF | 0.3283 |
| 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 | 2E-10 |
| Odds Ratio | 1.0700 [1.11-1.04] |
