Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5743708
rs5743708
0.020 GeneticVariation BEFREE R753Q SNP impairs TLR2-mediated immune recognition of HCV core and NS3 proteins. 20090572

2010

dbSNP: rs5743708
rs5743708
0.020 GeneticVariation BEFREE Homozygous TLR2 Arg753Gln polymorphism is associated with allograft failure and mortality after liver transplantation for chronic HCV. 17713436

2007

dbSNP: rs111200466
rs111200466
0.010 GeneticVariation BEFREE <b>Results:</b> While the rs12979860 IFNL3 T allele was found a good marker associated with HCV-outcome together with the rs111200466 TLR2 del variant, the rs10204525 PD-1.6 A allele was found to have an insignificant role in patients with HCV-related hepatic disorders. 30930876

2019

dbSNP: rs5743704
rs5743704
0.010 GeneticVariation BEFREE Here, we investigated whether single nucleotide polymorphisms (SNPs), rs4696480, rs5743708, rs5743704 and the -196 to -174 del/ins polymorphism of the TLR2 gene affect the risk for HCC in chronic hepatitis C. The study involved 189 and 192 HCV genotype 1 infected patients with and without HCC, respectively, as well as 347 healthy controls. 21500195

2012