rs885952
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs885952(A;A) |
| Make rs885952(A;G) |
| Make rs885952(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 31171713 |
| Gene | POU5F1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs885952 |
| dbSNP (classic) | rs885952 |
| ClinGen | rs885952 |
| ebi | rs885952 |
| HLI | rs885952 |
| Exac | rs885952 |
| Gnomad | rs885952 |
| Varsome | rs885952 |
| LitVar | rs885952 |
| Map | rs885952 |
| PheGenI | rs885952 |
| Biobank | rs885952 |
| 1000 genomes | rs885952 |
| hgdp | rs885952 |
| ensembl | rs885952 |
| geneview | rs885952 |
| scholar | rs885952 |
| rs885952 | |
| pharmgkb | rs885952 |
| gwascentral | rs885952 |
| openSNP | rs885952 |
| 23andMe | rs885952 |
| SNPshot | rs885952 |
| SNPdbe | rs885952 |
| MSV3d | rs885952 |
| GWAS Ctlg | rs885952 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 27596359] Identification of Novel OCT4 Genetic Variant Associated with the Risk of Chronic Hepatitis B in a Korean Population.
