rs568406
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs568406(C;C) |
| Make rs568406(C;G) |
| Make rs568406(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 165924036 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs568406 |
| dbSNP (classic) | rs568406 |
| ClinGen | rs568406 |
| ebi | rs568406 |
| HLI | rs568406 |
| Exac | rs568406 |
| Gnomad | rs568406 |
| Varsome | rs568406 |
| LitVar | rs568406 |
| Map | rs568406 |
| PheGenI | rs568406 |
| Biobank | rs568406 |
| 1000 genomes | rs568406 |
| hgdp | rs568406 |
| ensembl | rs568406 |
| geneview | rs568406 |
| scholar | rs568406 |
| rs568406 | |
| pharmgkb | rs568406 |
| gwascentral | rs568406 |
| openSNP | rs568406 |
| 23andMe | rs568406 |
| SNPshot | rs568406 |
| SNPdbe | rs568406 |
| MSV3d | rs568406 |
| GWAS Ctlg | rs568406 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26631030] Genetic variants in IL12 influence both hepatitis B virus clearance and HBV-related hepatocellular carcinoma development in a Chinese male population.
