Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The study highlighted the role of the SLC10A1 S267F variant in the loss of the ability to support HBV infection and taurocholate transport activity. 31177598

2019

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The S267F variant was found more frequently among HCs (16%) compared to HBV-infected (6%) and HBV-HDV co-infected patients (3%) (HBV patients vs HC: OR=0.32, P=0.00002 and HDV patients vs. HC: OR=0.17, P=0.018). 30685591

2019

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE Our results showed that rs2296651 polymorphism was associated with a decreased risk of susceptibility to HBV infection and the development of HCC. 31117968

2019

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE Viral and host predictors of relapse were evaluated, including hepatitis B virus (HBV) surface antigen (HBsAg) level, anti-HBV core antibody level, and presence of single-nucleotide polymorphisms in the genes encoding the receptors NTCP (rs2296651) and CTLA4 (rs231775) and in the 3' untranslated regions of the genes encoding HLA-DPA1 (rs3077) and HLA-DPB1 (rs9277535); posttherapy predictors of relapse were also investigated. 29300980

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The S267F variant for the HBV cell-entry receptor NTCP was associated with increased resistance to HBV infection and decreased risk for cirrhosis and liver cancer among those with chronic HBV infection. 29905807

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 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
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The p.Ser267Phe variant of sodium taurocholate cotransporting polypeptide (NTCP) supports HBV infection with a low efficiency. 30032030

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The S267F variant on the NTCP gene is independently associated with sustained normalization of ALT following treatment with PEG-IFN in patients with HBV infection who are HBeAg-positive. 28635613

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE Hepatitis B virus infection in Taiwan: The role of NTCP rs2296651 variant in relation to sex. 29660219

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE Analysis of hepatitis B virus preS1 variability and prevalence of the rs2296651 polymorphism in a Spanish population. 29456407

2018

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE In conclusion, the S267F variant of NTCP is clinically associated with a lower risk of chronic HBV infection and cirrhosis development, which implicates suppressing HBV entry could reduce the disease burden. 29247233

2017

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The role of SLC10A1 polymorphisms, particularly the Ser267Phe variant (rs2296651) in exon 4, has been frequently investigated in regard to risk of persistent HBV infection. 28429786

2017

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The S267F variant is absent among Moroccans regardless of chronic HBV infection status. 28125961

2017

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE Meta-analysis also showed that NTCP rs2296651-GA was inversely associated with HBV infection [OR(95%CI)=0.532(0.287-0.986), <i>p</i>=0.028, codominant] or HBV-related HCC [OR(95%CI)=0.701(0.564-0.872), <i>p</i>=0.001, recessive]. 29285260

2017

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE The p.Ser267Phe variant was associated with healthy status (P = 5.7 × 10(-23) , odds ratio = 0.36) irrespective of hepatitis B virus surface antibody status (P = 6.2 × 10(-21) and 1.5 × 10(-10) , respectively, when the cases were compared with hepatitis B virus surface antibody-positive and -negative controls). 25418280

2015

dbSNP: rs2296651
rs2296651
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation BEFREE These findings suggest that the rs2296651 polymorphism may predispose the susceptibility to and chronicity of HBV infection. 24735529

2014

dbSNP: rs201339654
rs201339654
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation BEFREE An exchange from arginine to glycine (as present in humans and great apes) at this position (R158G) alone was sufficient to achieve full transport-competing HBV myr-preS1-peptide binding and susceptibility for HBV/HDV infection. 29912972

2018

dbSNP: rs4646285
rs4646285
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation BEFREE The rs4646285 variants could influence the expression of NTCP at the level of transcription, and ultimately may be associated with HBV infection immune recovery. 29205714

2018

dbSNP: rs4646287
rs4646287
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation BEFREE We found a genetic variant (rs4646287) located in intron 1 of NTCP that may be associated with increased risk of HBV infection in Han Chinese. 26968990

2016

dbSNP: rs7154439
rs7154439
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation BEFREE The rs7154439 AA genotype was associated with HBV clearance, while the rs4646287 AA genotype was associated with HCC occurrence. 25010264

2014

dbSNP: rs943277
rs943277
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation BEFREE Furthermore, the frequency of rs943277-GA was positively correlated with HBV infection [adjusted OR(95%CI)=2.42(1.05-5.54), <i>p</i>=0.032, codominant]. 29285260

2017