rs7927997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7927997(C;C) |
| Make rs7927997(C;T) |
| Make rs7927997(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 76590331 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7927997 |
| dbSNP (classic) | rs7927997 |
| ClinGen | rs7927997 |
| ebi | rs7927997 |
| HLI | rs7927997 |
| Exac | rs7927997 |
| Gnomad | rs7927997 |
| Varsome | rs7927997 |
| LitVar | rs7927997 |
| Map | rs7927997 |
| PheGenI | rs7927997 |
| Biobank | rs7927997 |
| 1000 genomes | rs7927997 |
| hgdp | rs7927997 |
| ensembl | rs7927997 |
| geneview | rs7927997 |
| scholar | rs7927997 |
| rs7927997 | |
| pharmgkb | rs7927997 |
| gwascentral | rs7927997 |
| openSNP | rs7927997 |
| 23andMe | rs7927997 |
| SNPshot | rs7927997 |
| SNPdbe | rs7927997 |
| MSV3d | rs7927997 |
| GWAS Ctlg | rs7927997 |
| GMAF | 0.2723 |
| 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 | T |
| P-val | 6E-13 |
| Odds Ratio | 1.17 [1.12-1.22] |
