Rs12146962
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12146962 |
| PheGenI | rs12146962 |
| nextbio | rs12146962 |
| hapmap | rs12146962 |
| 1000 genomes | rs12146962 |
| hgdp | rs12146962 |
| ensembl | rs12146962 |
| gopubmed | rs12146962 |
| geneview | rs12146962 |
| scholar | rs12146962 |
| rs12146962 | |
| pharmgkb | rs12146962 |
| gwascentral | rs12146962 |
| openSNP | rs12146962 |
| 23andMe | rs12146962 |
| 23andMe all | rs12146962 |
| SNP Nexus | |
| SNPshot | rs12146962 |
| SNPdbe | rs12146962 |
| MSV3d | rs12146962 |
| Chromosome | 14 |
| Orientation | plus |
| GMAF | 0.4245 |
| Position | 33381098 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs12146962(C;C) |
| Make rs12146962(C;T) |
| Make rs12146962(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 22138694] |
| Trait | |
| Title | A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis. |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | 1.1400 None |
| GET Evidence | |
|---|---|
| rs12146962 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.429688 |
| summary | |
