Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1798802
rs1798802
0.010 GeneticVariation BEFREE The results showed rs1798802 (AA compared with GG: <i>P</i>=0.044, OR=0.72) and rs2293303 (TT compared with CC: <i>P</i>=0.002, OR=2.86; recessive model: <i>P</i>=0.006, OR=2.91; T compared with C: <i>P</i>=0.004, OR=1.19) polymorphisms were associated with overall cancer risk. 28963373

2017

dbSNP: rs2293303
rs2293303
0.010 GeneticVariation BEFREE The results showed rs1798802 (AA compared with GG: <i>P</i>=0.044, OR=0.72) and rs2293303 (TT compared with CC: <i>P</i>=0.002, OR=2.86; recessive model: <i>P</i>=0.006, OR=2.91; T compared with C: <i>P</i>=0.004, OR=1.19) polymorphisms were associated with overall cancer risk. 28963373

2017

dbSNP: rs4135385
rs4135385
0.010 GeneticVariation BEFREE The polymorphism rs4135385 of CTNNB1 genotype GA was associated with a higher risk for Stage III + IV HCC (modified Union for International Cancer Control) (P = 0.001, OR = 2.238).Genetic polymorphisms in the WNT2 and CTNNB1 genes were closely associated with HCC risk and progression in a Chinese Han population. 28328801

2017