rs11978472
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11978472(A;A) |
| Make rs11978472(A;C) |
| Make rs11978472(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 82210237 |
| Gene | CACNA2D1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11978472 |
| dbSNP (classic) | rs11978472 |
| ClinGen | rs11978472 |
| ebi | rs11978472 |
| HLI | rs11978472 |
| Exac | rs11978472 |
| Gnomad | rs11978472 |
| Varsome | rs11978472 |
| LitVar | rs11978472 |
| Map | rs11978472 |
| PheGenI | rs11978472 |
| Biobank | rs11978472 |
| 1000 genomes | rs11978472 |
| hgdp | rs11978472 |
| ensembl | rs11978472 |
| geneview | rs11978472 |
| scholar | rs11978472 |
| rs11978472 | |
| pharmgkb | rs11978472 |
| gwascentral | rs11978472 |
| openSNP | rs11978472 |
| 23andMe | rs11978472 |
| SNPshot | rs11978472 |
| SNPdbe | rs11978472 |
| MSV3d | rs11978472 |
| GWAS Ctlg | rs11978472 |
| GMAF | 0.3691 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23665963 ]
|
| Trait | Crohn's disease (need for surgery) |
| Title | Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease. |
| Risk Allele | |
| P-val | 6E-6 |
| Odds Ratio | 2.00 [1.43-2.50] |
