Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE In addition, our findings further suggest that the combination of MDM2 SNP 309 and TP53 Arg72Pro genotypes confers higher risk to develop HCC. 24376578

2013

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE This study aimed to assess whether polymorphisms in the single-nucleotide polymorphism miR-34b/c T>C (rs4938723) and TP53 Arg72Pro (rs1042522) increase the risk of HCC and influence outcome in patients with HCC. 23632240

2013

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE The study on p53 Arg72Pro and XRCC1 Arg399Gln polymorphism in HCC patients demonstrated differences in allele frequencies compared to their controls. 23053887

2013

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE In subgroup analysis by ethnicity, the pooled results suggested that the p53 codon 72 Arg/Pro polymorphism was associated with an increased risk of HCC in Asians and Caucasians (for Asians, ORProPro vs. ArgArg + ArgPro=1.17 (95 % CI, 1.02-1.34), P OR=0.025; for Caucasians, ORProPro vs. ArgArg = 1.65 (95 % CI, 1.07-2.56), P OR=0.025; ORProPro vs. ArgArg + ArgPro=1.74 (95 % CI, 1.14-2.66), P OR=0.010). 23564481

2013

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE In addition, our findings further suggest that the combination of MDM2 SNP 309 and TP53 Arg72Pro genotypes confers higher risk to develop HCC. 24376578

2013

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE This study aimed to assess whether polymorphisms in the single-nucleotide polymorphism miR-34b/c T>C (rs4938723) and TP53 Arg72Pro (rs1042522) increase the risk of HCC and influence outcome in patients with HCC. 23632240

2013

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE Two single nucleotide polymorphisms (SNPs) in the gene loci of p53 pathway, p53 codon 72 Arg72Pro and MDM2 SNP309 (T > G), have been shown to cause perturbation of p53 function, but the effect of the two SNPs on the risk of hepatocellular carcinoma (HCC) remains inconsistent. 23292895

2013

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Two single nucleotide polymorphisms (SNPs) in the gene loci of p53 pathway, p53 codon 72 Arg72Pro and MDM2 SNP309 (T > G), have been shown to cause perturbation of p53 function, but the effect of the two SNPs on the risk of hepatocellular carcinoma (HCC) remains inconsistent. 23292895

2013

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE This study aimed to assess whether polymorphisms in the single-nucleotide polymorphism miR-34b/c T>C (rs4938723) and TP53 Arg72Pro (rs1042522) increase the risk of HCC and influence outcome in patients with HCC. 23632240

2013

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE In addition, our findings further suggest that the combination of MDM2 SNP 309 and TP53 Arg72Pro genotypes confers higher risk to develop HCC. 24376578

2013

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE In subgroup analysis by ethnicity, the pooled results suggested that the p53 codon 72 Arg/Pro polymorphism was associated with an increased risk of HCC in Asians and Caucasians (for Asians, ORProPro vs. ArgArg + ArgPro=1.17 (95 % CI, 1.02-1.34), P OR=0.025; for Caucasians, ORProPro vs. ArgArg = 1.65 (95 % CI, 1.07-2.56), P OR=0.025; ORProPro vs. ArgArg + ArgPro=1.74 (95 % CI, 1.14-2.66), P OR=0.010). 23564481

2013

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE The study on p53 Arg72Pro and XRCC1 Arg399Gln polymorphism in HCC patients demonstrated differences in allele frequencies compared to their controls. 23053887

2013

dbSNP: rs1064793929
rs1064793929
0.010 GeneticVariation BEFREE In contrast, the β-catenin mutation was associ</span>ated with better prognosis in both S100P-positive and -negative HCC</span>s. 23785431

2013

dbSNP: rs28934571
rs28934571
0.800 GeneticVariation BEFREE Overall, these results support the preferential occurrence of R249S-mutated DNA in HCC developing in the absence of cirrhosis in a context of HBV chronic infection. 22675488

2012

dbSNP: rs28934571
rs28934571
0.800 GeneticVariation BEFREE These findings suggest that in HCC from The Gambia, complete HBX sequences are often associated with the presence of TP53 R249S mutation. 22759751

2012

dbSNP: rs121912656
rs121912656
0.710 GeneticVariation BEFREE Furthermore, p53(G245D) was shown to have a similar pattern of subcellular localization to ZBP-89 in tissues of HCC patients in Hong Kong. 22214764

2012

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Meta-analyses of available data suggest an obvious association between the TP53 Arg72Pro and HCC risk in Caucasians. 23167333

2012

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Our data shows that the Pro/Pro genotype of the p53 Arg72Pro polymorphism is associated with increased risk of HCC development in this Turkish population (OR = 3.20, 95% CI: 1.24-8.22, P = 0.02). 21607615

2012

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE There was no evidence for any association with early age of HCC onset when deleterious alleles of MDM2 SNP309 and TP53 Arg72Pro where present. 22180176

2012

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE Our data shows that the Pro/Pro genotype of the p53 Arg72Pro polymorphism is associated with increased risk of HCC development in this Turkish population (OR = 3.20, 95% CI: 1.24-8.22, P = 0.02). 21607615

2012

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE Meta-analyses of available data suggest an obvious association between the TP53 Arg72Pro and HCC risk in Caucasians. 23167333

2012

dbSNP: rs1131691014
rs1131691014
0.100 GeneticVariation BEFREE There was no evidence for any association with early age of HCC onset when deleterious alleles of MDM2 SNP309 and TP53 Arg72Pro where present. 22180176

2012

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Our data shows that the Pro/Pro genotype of the p53 Arg72Pro polymorphism is associated with increased risk of HCC development in this Turkish population (OR = 3.20, 95% CI: 1.24-8.22, P = 0.02). 21607615

2012

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE There was no evidence for any association with early age of HCC onset when deleterious alleles of MDM2 SNP309 and TP53 Arg72Pro where present. 22180176

2012

dbSNP: rs878854066
rs878854066
0.100 GeneticVariation BEFREE Meta-analyses of available data suggest an obvious association between the TP53 Arg72Pro and HCC risk in Caucasians. 23167333

2012