rs11693697
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11693697(C;C) |
| Make rs11693697(C;T) |
| Make rs11693697(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 102299202 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11693697 |
| dbSNP (classic) | rs11693697 |
| ClinGen | rs11693697 |
| ebi | rs11693697 |
| HLI | rs11693697 |
| Exac | rs11693697 |
| Gnomad | rs11693697 |
| Varsome | rs11693697 |
| LitVar | rs11693697 |
| Map | rs11693697 |
| PheGenI | rs11693697 |
| Biobank | rs11693697 |
| 1000 genomes | rs11693697 |
| hgdp | rs11693697 |
| ensembl | rs11693697 |
| geneview | rs11693697 |
| scholar | rs11693697 |
| rs11693697 | |
| pharmgkb | rs11693697 |
| gwascentral | rs11693697 |
| openSNP | rs11693697 |
| 23andMe | rs11693697 |
| SNPshot | rs11693697 |
| SNPdbe | rs11693697 |
| MSV3d | rs11693697 |
| GWAS Ctlg | rs11693697 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23999434 ]
|
| Trait | Serum protein levels (sST2) |
| Title | Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. |
| Risk Allele | C |
| P-val | 7E-11 |
| Odds Ratio | .08 [0.06-0.1] unit decrease |
