rs2149085
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2149085(C;C) |
| Make rs2149085(C;T) |
| Make rs2149085(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 166957622 |
| Gene | RNASET2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2149085 |
| dbSNP (classic) | rs2149085 |
| ClinGen | rs2149085 |
| ebi | rs2149085 |
| HLI | rs2149085 |
| Exac | rs2149085 |
| Gnomad | rs2149085 |
| Varsome | rs2149085 |
| LitVar | rs2149085 |
| Map | rs2149085 |
| PheGenI | rs2149085 |
| Biobank | rs2149085 |
| 1000 genomes | rs2149085 |
| hgdp | rs2149085 |
| ensembl | rs2149085 |
| geneview | rs2149085 |
| scholar | rs2149085 |
| rs2149085 | |
| pharmgkb | rs2149085 |
| gwascentral | rs2149085 |
| openSNP | rs2149085 |
| 23andMe | rs2149085 |
| SNPshot | rs2149085 |
| SNPdbe | rs2149085 |
| MSV3d | rs2149085 |
| GWAS Ctlg | rs2149085 |
| GMAF | 0.393 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23850713] |
| Trait | Crohn's disease |
| Title | Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. |
| Risk Allele | T |
| P-val | 8E-12 |
| Odds Ratio | 1.34 [1.23-1.45] |
