Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2296651
rs2296651
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
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
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
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
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
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