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rs8105790

From SNPedia

Orientationplus
Stabilizedplus
Make rs8105790(C;C)
Make rs8105790(C;T)
Make rs8105790(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position39241861
GeneIL28B
is asnp
is mentioned by
dbSNPrs8105790
ebirs8105790
HLIrs8105790
Exacrs8105790
Varsomers8105790
Maprs8105790
PheGenIrs8105790
hapmaprs8105790
1000 genomesrs8105790
hgdprs8105790
ensemblrs8105790
gopubmedrs8105790
geneviewrs8105790
scholarrs8105790
googlers8105790
pharmgkbrs8105790
gwascentralrs8105790
openSNPrs8105790
23andMers8105790
23andMe allrs8105790
SNP Nexus

SNPshotrs8105790
SNPdbers8105790
MSV3drs8105790
GWAS Ctlgrs8105790
GMAF0.1731
Max Magnitude
? (C;C) (C;T) (T;T) 28

[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.


GET Evidence
rs8105790
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.233871
summary



[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