Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123341
rs398123341
C 0.700 CausalMutation CLINVAR

dbSNP: rs398123342
rs398123342
TG 0.700 CausalMutation CLINVAR

dbSNP: rs745554420
rs745554420
A 0.700 CausalMutation CLINVAR

dbSNP: rs11615
rs11615
0.010 GeneticVariation BEFREE From six eligible articles in our study, we found that for ERCC1 rs11615 polymorphism, a significant association was detected between the chemotherapy response and the polymorphism under all three models (dominant model: OR = 2.015, P = 0.005; recessive model: OR = 1.791, P = 0.003; allelic model: OR = 1.677, P = 0.003), and OS patients carrying C allele in rs11615 polymorphism were more likely to response to chemotherapy. 28388903

2017

dbSNP: rs13181
rs13181
0.010 GeneticVariation BEFREE With respect to ERCC2 rs13181 polymorphism, this polymorphism was not correlated with the response to chemotherapy for OS patients under all three models. 28388903

2017

dbSNP: rs1799793
rs1799793
0.010 GeneticVariation BEFREE In terms of ERCC2 rs1799793 polymorphism, this polymorphism was significantly associated with the response to chemotherapy for OS patients under recessive model (OR = 1.337, P = 0.036), and patients with AG + AA genotype in rs1799793 polymorphism were more appropriate to receive chemotherapy. 28388903

2017

dbSNP: rs324148
rs324148
0.010 GeneticVariation BEFREE Post-induction overall survival (OS) significantly decreased in patients with the CC genotype of rs324148 compared with CT and TT genotypes (hazard ratio [HR] = 2.997 [95% confidence interval (CI): 1.71-5.27]). 25398670

2014