Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7453920
rs7453920
HLA-DQB2
0.720 GeneticVariation GWASCAT A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081

2013
dbSNP: rs7549785
rs7549785
FCER1A
0.710 GeneticVariation BEFREE FCER1A (rs7549785) and possibly POLR3G (rs7712322) are shown to be associated with peginterferon alfa-2a response in adult patients with chronic hepatitis B. 30972912

2019
dbSNP: rs7549785
rs7549785
FCER1A
0.710 GeneticVariation GWASCAT FCER1A (rs7549785) and possibly POLR3G (rs7712322) are shown to be associated with peginterferon alfa-2a response in adult patients with chronic hepatitis B. 30972912

2019
dbSNP: rs61886277
rs61886277
PLCE1
T 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies Genetic Variants Associated With Early and Sustained Response to (Pegylated) Interferon in Chronic Hepatitis B Patients: The GIANT-B Study. 30715261

2019
dbSNP: rs78900671
rs78900671
COL22A1
C 0.700 GeneticVariation GWASCAT Genome-wide Association Study Identifies Genetic Variants Associated With Early and Sustained Response to (Pegylated) Interferon in Chronic Hepatitis B Patients: The GIANT-B Study. 30715261

2019
dbSNP: rs9287655
rs9287655
NBAS
0.700 GeneticVariation GWASCAT Genetic variation in FCER1A predicts peginterferon alfa-2a-induced hepatitis B surface antigen clearance in East Asian patients with chronic hepatitis B. 30972912

2019
dbSNP: rs12614
rs12614
CFB ; CYP21A2
T 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs1419881
rs1419881
TCF19
G 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs1883832
rs1883832
CD40
T 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs2853953
rs2853953 		A 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs3130542
rs3130542 		A 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs378352
rs378352
HLA-DOA
T 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs422951
rs422951
NOTCH4
G 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs652888
rs652888
CYP21A2 ; EHMT2 ; EHMT2-AS1 ; LOC107986588
G 0.700 GeneticVariation GWASCAT Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. 25802187

2015
dbSNP: rs7756516
rs7756516
HLA-DQB2
T 0.700 GeneticVariation GWASCAT A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. 24940741

2014
dbSNP: rs9276370
rs9276370
HLA-DQA2
T 0.700 GeneticVariation GWASCAT A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. 24940741

2014
dbSNP: rs9366816
rs9366816
HLA-DPA3 ; LOC105375021
T 0.700 GeneticVariation GWASCAT A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. 24940741

2014
dbSNP: rs9366816
rs9366816
HLA-DPA3 ; LOC105375021
C 0.700 GeneticVariation GWASCAT A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. 24940741

2014
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE Association of the S267F variant on NTCP gene and treatment response to pegylated interferon in patients with chronic hepatitis B: a multicentre study. 28635613

2018
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE Intriguingly, ten individuals were identified as S267F homozygotes in population studies of chronic hepatitis B (CHB) patients. 30032030

2018
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE The S267F variant may be a protective factor to resist chronic hepatitis B progression which showed a higher bile acid level in Chinese Han chronic HBV infection patients. 29205714

2018
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE In this study, we aimed to evaluate the prevalence of S267F polymorphism in Korean patients with chronic hepatitis B (CHB) and its association with disease progression and potential viral evolution in the preS1 domain of HBV. 29247233

2017
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE The rs2296651 (S267F) variant on NTCP (SLC10A1) is inversely associated with chronic hepatitis B and progression to cirrhosis and hepatocellular carcinoma in patients with chronic hepatitis B. 26642861

2016
dbSNP: rs2296651
rs2296651
SLC10A1
0.060 GeneticVariation BEFREE The p.Ser267Phe NTCP variant is significantly associated with resistance to chronic hepatitis B and a lower incidence of acute-on-chronic liver failure. 25418280

2015
dbSNP: rs12979860
rs12979860
IFNL4
0.050 GeneticVariation BEFREE IL28B genetic variations (rs12979860) were genotyped by pyrosequencing of DNA samples from 137 individuals with chronic HBV infection [50 inactive carriers (IC), 34 chronic hepatitis B (CHB), 27 cirrhosis, 26 hepatocellular carcinoma (HCC)], and 19 healthy controls. 25837166

2015