rs11766298
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs11766298(C;T) |
| Make rs11766298(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 129365006 |
| Gene | AHCYL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11766298 |
| dbSNP (classic) | rs11766298 |
| ClinGen | rs11766298 |
| ebi | rs11766298 |
| HLI | rs11766298 |
| Exac | rs11766298 |
| Gnomad | rs11766298 |
| Varsome | rs11766298 |
| LitVar | rs11766298 |
| Map | rs11766298 |
| PheGenI | rs11766298 |
| Biobank | rs11766298 |
| 1000 genomes | rs11766298 |
| hgdp | rs11766298 |
| ensembl | rs11766298 |
| geneview | rs11766298 |
| scholar | rs11766298 |
| rs11766298 | |
| pharmgkb | rs11766298 |
| gwascentral | rs11766298 |
| openSNP | rs11766298 |
| 23andMe | rs11766298 |
| SNPshot | rs11766298 |
| SNPdbe | rs11766298 |
| MSV3d | rs11766298 |
| GWAS Ctlg | rs11766298 |
| GMAF | 0.02158 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22890011 ]
|
| Trait | Response to fenofibrate |
| Title | Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate. |
| Risk Allele | T |
| P-val | 4E-9 |
| Odds Ratio | 4.41 [2.96-5.86] unit increase |
