rs10159477
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10159477(A;A) |
| Make rs10159477(A;G) |
| Make rs10159477(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 69340132 |
| Gene | HK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10159477 |
| dbSNP (classic) | rs10159477 |
| ClinGen | rs10159477 |
| ebi | rs10159477 |
| HLI | rs10159477 |
| Exac | rs10159477 |
| Gnomad | rs10159477 |
| Varsome | rs10159477 |
| LitVar | rs10159477 |
| Map | rs10159477 |
| PheGenI | rs10159477 |
| Biobank | rs10159477 |
| 1000 genomes | rs10159477 |
| hgdp | rs10159477 |
| ensembl | rs10159477 |
| geneview | rs10159477 |
| scholar | rs10159477 |
| rs10159477 | |
| pharmgkb | rs10159477 |
| gwascentral | rs10159477 |
| openSNP | rs10159477 |
| 23andMe | rs10159477 |
| SNPshot | rs10159477 |
| SNPdbe | rs10159477 |
| MSV3d | rs10159477 |
| GWAS Ctlg | rs10159477 |
| GMAF | 0.09871 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23222517 ]
|
| Trait | Red blood cell traits |
| Title | Seventy-five genetic loci influencing the human red blood cell. |
| Risk Allele | A |
| P-val | 4E-20 |
| Odds Ratio | .09 [0.067-0.107] unit increase |
[PMID 19853236] Sequence variants in three loci influence monocyte counts and erythrocyte volume.
