Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE The rs4803217 SNP is a strong, independent and superior predictor of SVR and relapse in HCV genotype 1 infected CHC patients treated with PEG-IFN-α and RBV. 28638221

2017

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE Among AA participants, associations were stronger for IFNL4-ΔG/TT than rs4803217 for undetectable HCV RNA at week 24 in Virahep-C (p=0.03) and week 20 in HALT-C (p=0.03), as well as for spontaneous HCV clearance (p=0.048). 26186989

2015

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE We analyzed a variant (rs4803217 G/T) located within the IFNL3 mRNA 3' untranslated region (UTR); the G allele (protective allele) is associated with elevated therapeutic HCV clearance. 26531896

2015

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE This analysis included the two strongest tag predictors for HCV clearance, rs8099917 and rs12979860, and four causal variants (rs4803219, rs28416813, rs8103142, and rs4803217) located in the IL28B promoter, coding, and 3'-untranslated regions. 22328925

2012