Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5744174
rs5744174
TLR5
0.020 GeneticVariation BEFREE From all three analyzed SNPs association of TLR5 (rs5744174) with CHB is the most significant. 29276096

2018
dbSNP: rs5744174
rs5744174
TLR5
0.020 GeneticVariation BEFREE Frequency of TT genotype of TLR5 rs5744174 in patients positive for HBeAg was increased from 53.2% in patients with CHB to 74.1% in those with HCC (p = 0.024). 28543911

2017