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rs7248668

From SNPedia

Orientationplus
Stabilizedplus
Make rs7248668(A;A)
Make rs7248668(A;G)
Make rs7248668(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position39253181
GeneRFX6
is asnp
is mentioned by
dbSNPrs7248668
ebirs7248668
HLIrs7248668
Exacrs7248668
Varsomers7248668
Maprs7248668
PheGenIrs7248668
hapmaprs7248668
1000 genomesrs7248668
hgdprs7248668
ensemblrs7248668
gopubmedrs7248668
geneviewrs7248668
scholarrs7248668
googlers7248668
pharmgkbrs7248668
gwascentralrs7248668
openSNPrs7248668
23andMers7248668
23andMe allrs7248668
SNP Nexus

SNPshotrs7248668
SNPdbers7248668
MSV3drs7248668
GWAS Ctlgrs7248668
GMAF0.1382
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19749757] Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C



GET Evidence
rs7248668
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.15625
summary



[PMID 23103287] IL28B polymorphisms are associated with severity of liver disease in human immunodeficiency virus (HIV) patients coinfected with hepatitis C virus.


[PMID 23135173] Analysis of IL28B alleles with virologic response patterns and plasma cytokine levels in HIV/HCV-coinfected patients.


[PMID 24118788] Genetic variation in interleukin 28B and correlation with chronic hepatitis B virus infection in Saudi Arabian patients