SLC10A1, solute carrier family 10 member 1, 6554

N. diseases: 54; N. variants: 7
Disease: Hepatitis B, Chronic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 GeneticVariation disease 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
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 GeneticVariation disease BEFREE Effect of S267F variant of NTCP on the patients with chronic hepatitis B. 29247233 2017
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 Biomarker disease BEFREE NTCP-targeted therapy has potential for regulating HBV infection in patients with chronic hepatitis B. 27278060 2016
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 GeneticVariation disease 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
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 GeneticVariation disease 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
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.060 GeneticVariation disease BEFREE Association of genetic variation of sodium taurocholate cotransporting polypeptide with chronic hepatitis B virus infection. 24735529 2014