rs424971
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs424971(C;C) |
| Make rs424971(C;T) |
| Make rs424971(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 85912844 |
| Gene | IRF8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs424971 |
| dbSNP (classic) | rs424971 |
| ClinGen | rs424971 |
| ebi | rs424971 |
| HLI | rs424971 |
| Exac | rs424971 |
| Gnomad | rs424971 |
| Varsome | rs424971 |
| LitVar | rs424971 |
| Map | rs424971 |
| PheGenI | rs424971 |
| Biobank | rs424971 |
| 1000 genomes | rs424971 |
| hgdp | rs424971 |
| ensembl | rs424971 |
| geneview | rs424971 |
| scholar | rs424971 |
| rs424971 | |
| pharmgkb | rs424971 |
| gwascentral | rs424971 |
| openSNP | rs424971 |
| 23andMe | rs424971 |
| SNPshot | rs424971 |
| SNPdbe | rs424971 |
| MSV3d | rs424971 |
| GWAS Ctlg | rs424971 |
| GMAF | 0.4674 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23314186 ]
|
| Trait | Monocyte count |
| Title | Genetic variation associated with circulating monocyte count in the eMERGE Network. |
| Risk Allele | G |
| P-val | 3E-16 |
| Odds Ratio | .22 unit decrease |
