rs8105790
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8105790(C;C) |
| Make rs8105790(C;T) |
| Make rs8105790(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 39241861 |
| Gene | IL28B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8105790 |
| dbSNP (classic) | rs8105790 |
| ClinGen | rs8105790 |
| ebi | rs8105790 |
| HLI | rs8105790 |
| Exac | rs8105790 |
| Gnomad | rs8105790 |
| Varsome | rs8105790 |
| LitVar | rs8105790 |
| Map | rs8105790 |
| PheGenI | rs8105790 |
| Biobank | rs8105790 |
| 1000 genomes | rs8105790 |
| hgdp | rs8105790 |
| ensembl | rs8105790 |
| geneview | rs8105790 |
| scholar | rs8105790 |
| rs8105790 | |
| pharmgkb | rs8105790 |
| gwascentral | rs8105790 |
| openSNP | rs8105790 |
| 23andMe | rs8105790 |
| SNPshot | rs8105790 |
| SNPdbe | rs8105790 |
| MSV3d | rs8105790 |
| GWAS Ctlg | rs8105790 |
| GMAF | 0.1731 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 19749757] Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C
[PMID 21254157] Role of interleukin-28B polymorphisms in the treatment of hepatitis C virus genotype 2 infection in Asian patients.
[PMID 22329371] IL28B genetic variants and gender are associated with spontaneous clearance of hepatitis C virus infection.
[PMID 24118788] Genetic variation in interleukin 28B and correlation with chronic hepatitis B virus infection in Saudi Arabian patients
[PMID 24840315] Interleukin-28 gene polymorphisms may contribute to HBsAg persistence and the development of HBeAg-negative chronic hepatitis B
