rs11712165
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11712165(G;G) |
| Make rs11712165(G;T) |
| Make rs11712165(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 119399949 |
| Gene | ARHGAP31 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11712165 |
| dbSNP (classic) | rs11712165 |
| ClinGen | rs11712165 |
| ebi | rs11712165 |
| HLI | rs11712165 |
| Exac | rs11712165 |
| Gnomad | rs11712165 |
| Varsome | rs11712165 |
| LitVar | rs11712165 |
| Map | rs11712165 |
| PheGenI | rs11712165 |
| Biobank | rs11712165 |
| 1000 genomes | rs11712165 |
| hgdp | rs11712165 |
| ensembl | rs11712165 |
| geneview | rs11712165 |
| scholar | rs11712165 |
| rs11712165 | |
| pharmgkb | rs11712165 |
| gwascentral | rs11712165 |
| openSNP | rs11712165 |
| 23andMe | rs11712165 |
| SNPshot | rs11712165 |
| SNPdbe | rs11712165 |
| MSV3d | rs11712165 |
| GWAS Ctlg | rs11712165 |
| GMAF | 0.3035 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20190752 ]
|
| Trait | Celiac disease |
| Title | Multiple common variants for celiac disease influencing immune gene expression |
| Risk Allele | C |
| P-val | 8E-9 |
| Odds Ratio | 1.13 [1.08-1.17] |
