rs6569992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6569992(A;A) |
| Make rs6569992(A;G) |
| Make rs6569992(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 135131014 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6569992 |
| dbSNP (classic) | rs6569992 |
| ClinGen | rs6569992 |
| ebi | rs6569992 |
| HLI | rs6569992 |
| Exac | rs6569992 |
| Gnomad | rs6569992 |
| Varsome | rs6569992 |
| LitVar | rs6569992 |
| Map | rs6569992 |
| PheGenI | rs6569992 |
| Biobank | rs6569992 |
| 1000 genomes | rs6569992 |
| hgdp | rs6569992 |
| ensembl | rs6569992 |
| geneview | rs6569992 |
| scholar | rs6569992 |
| rs6569992 | |
| pharmgkb | rs6569992 |
| gwascentral | rs6569992 |
| openSNP | rs6569992 |
| 23andMe | rs6569992 |
| SNPshot | rs6569992 |
| SNPdbe | rs6569992 |
| MSV3d | rs6569992 |
| GWAS Ctlg | rs6569992 |
| GMAF | 0.1873 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20927387 ]
|
| Trait | |
| Title | A genome-wide association study of red blood cell traits using the electronic medical record |
| Risk Allele | A |
| P-val | 3E-8 |
| Odds Ratio | 0.75 [0.48-1.02] unit increase |
