rs11190141
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11190141(C;C) |
| Make rs11190141(C;T) |
| Make rs11190141(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 99532633 |
| Gene | LINC01475, NKX2-3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11190141 |
| dbSNP (classic) | rs11190141 |
| ClinGen | rs11190141 |
| ebi | rs11190141 |
| HLI | rs11190141 |
| Exac | rs11190141 |
| Gnomad | rs11190141 |
| Varsome | rs11190141 |
| LitVar | rs11190141 |
| Map | rs11190141 |
| PheGenI | rs11190141 |
| Biobank | rs11190141 |
| 1000 genomes | rs11190141 |
| hgdp | rs11190141 |
| ensembl | rs11190141 |
| geneview | rs11190141 |
| scholar | rs11190141 |
| rs11190141 | |
| pharmgkb | rs11190141 |
| gwascentral | rs11190141 |
| openSNP | rs11190141 |
| 23andMe | rs11190141 |
| SNPshot | rs11190141 |
| SNPdbe | rs11190141 |
| MSV3d | rs11190141 |
| GWAS Ctlg | rs11190141 |
| GMAF | 0.4275 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 22412388 ]
|
| Trait | |
| Title | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. |
| Risk Allele | C |
| P-val | 5E-7 |
| Odds Ratio | 1.3400 None |
