rs17043947
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17043947(C;C) |
| Make rs17043947(C;T) |
| Make rs17043947(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 22514115 |
| Gene | LOC105374322 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17043947 |
| dbSNP (classic) | rs17043947 |
| ClinGen | rs17043947 |
| ebi | rs17043947 |
| HLI | rs17043947 |
| Exac | rs17043947 |
| Gnomad | rs17043947 |
| Varsome | rs17043947 |
| LitVar | rs17043947 |
| Map | rs17043947 |
| PheGenI | rs17043947 |
| Biobank | rs17043947 |
| 1000 genomes | rs17043947 |
| hgdp | rs17043947 |
| ensembl | rs17043947 |
| geneview | rs17043947 |
| scholar | rs17043947 |
| rs17043947 | |
| pharmgkb | rs17043947 |
| gwascentral | rs17043947 |
| openSNP | rs17043947 |
| 23andMe | rs17043947 |
| SNPshot | rs17043947 |
| SNPdbe | rs17043947 |
| MSV3d | rs17043947 |
| GWAS Ctlg | rs17043947 |
| GMAF | 0.1102 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20707712 ]
|
| Trait | |
| Title | A genome-wide association study of self-rated health |
| Risk Allele | T |
| P-val | 2E-7 |
| Odds Ratio | 0.07 [NR] unit decrease |
