rs58542926, TM6SF2

N. diseases: 42
Disease: Fatty Liver Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
0.050 GeneticVariation BEFREE Decreased liver production/secretion of VLDL, decreased cholesterol and TGs in VLDL/LDL particles in serum, and increased tyrosine levels identify possible mechanisms by which rs58542926-T exerts its effects on increasing risk of fatty liver disease, decreasing cardiovascular disease, and increasing diabetes risk, respectively. 28539357 2017
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
0.050 GeneticVariation BEFREE Interestingly, patients harbouring the TM6SF2 rs58542926 T allele that predispose to NAFLD/NASH had higher LBP level. 28464257 2017
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
0.050 GeneticVariation BEFREE Role of TM6SF2 rs58542926 in the pathogenesis of nonalcoholic pediatric fatty liver disease: A multiethnic study. 26457389 2016
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
0.050 GeneticVariation BEFREE Carriers of the TM6SF2 E167K variant are more susceptible to progressive NASH, but are protected against cardiovascular disease. 25251399 2015
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
0.050 GeneticVariation BEFREE Recently, genome-wide association studies led to the identification of the major inherited determinants of hepatic fat accumulation: patatin-like phospholipase domain-containing 3 (PNPLA3) I148M gene and transmembrane 6 superfamily member 2 (TM6SF2) E167K gene variants, involved in lipid droplets remodelling and very low-density lipoproteins secretion, are the major determinants of interindividual differences in liver steatosis, and susceptibility to progressive NASH. 26273621 2015