rs2146807
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2146807(C;C) |
| Make rs2146807(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 44318290 |
| Gene | CXCL12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2146807 |
| dbSNP (classic) | rs2146807 |
| ClinGen | rs2146807 |
| ebi | rs2146807 |
| HLI | rs2146807 |
| Exac | rs2146807 |
| Gnomad | rs2146807 |
| Varsome | rs2146807 |
| LitVar | rs2146807 |
| Map | rs2146807 |
| PheGenI | rs2146807 |
| Biobank | rs2146807 |
| 1000 genomes | rs2146807 |
| hgdp | rs2146807 |
| ensembl | rs2146807 |
| geneview | rs2146807 |
| scholar | rs2146807 |
| rs2146807 | |
| pharmgkb | rs2146807 |
| gwascentral | rs2146807 |
| openSNP | rs2146807 |
| 23andMe | rs2146807 |
| SNPshot | rs2146807 |
| SNPdbe | rs2146807 |
| MSV3d | rs2146807 |
| GWAS Ctlg | rs2146807 |
| GMAF | 0.1575 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18979498
] rs2146807 association with the fatality of acute coronary event
