rs2228467
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs2228467(C;C) |
| Make rs2228467(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 42864624 |
| Gene | ACKR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228467 |
| dbSNP (classic) | rs2228467 |
| ClinGen | rs2228467 |
| ebi | rs2228467 |
| HLI | rs2228467 |
| Exac | rs2228467 |
| Gnomad | rs2228467 |
| Varsome | rs2228467 |
| LitVar | rs2228467 |
| Map | rs2228467 |
| PheGenI | rs2228467 |
| Biobank | rs2228467 |
| 1000 genomes | rs2228467 |
| hgdp | rs2228467 |
| ensembl | rs2228467 |
| geneview | rs2228467 |
| scholar | rs2228467 |
| rs2228467 | |
| pharmgkb | rs2228467 |
| gwascentral | rs2228467 |
| openSNP | rs2228467 |
| 23andMe | rs2228467 |
| SNPshot | rs2228467 |
| SNPdbe | rs2228467 |
| MSV3d | rs2228467 |
| GWAS Ctlg | rs2228467 |
| GMAF | 0.02984 |
| 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 | 2E-7 |
| Odds Ratio | .30 unit increase |
