Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1003897973
rs1003897973
0.010 GeneticVariation BEFREE We failed to confirm earlier reports of increased cervical cancer susceptibility in women who harbor the p53 P72R allele. 12142377

2002

dbSNP: rs1007541
rs1007541
0.010 GeneticVariation BEFREE Stratification according to FIGO staging revealed that the minor allele of rs1007541 was more frequent among advanced tumor stage patients, with 11-fold increased risk of CC [P < 0.0001; OR (95 % CI) = 11.32 (7.46-17.18)]. 27844329

2017

dbSNP: rs1030389
rs1030389
0.010 GeneticVariation BEFREE Analysis of the SNPs after stratification based on CC clinical stage and subtype revealed that rs1048512, rs6659346, rs217727, rs9931702, and rs9302648 were associated with CC risk in clinical stages I-II; rs2862833, rs2732044, rs1030389, and rs1045935 were associated with CC risk in clinical stages III-IV; and rs217727, rs9931702, and rs9302648 were associated with CC risk in squamous carcinomas. 27765929

2016

dbSNP: rs1041981
rs1041981
0.010 GeneticVariation BEFREE A significant association of CxCa with various polymorphisms was observed: rs1800797 in the IL-6 gene (odds ratio [OR] = 0.88, 95% confidence intervals [CI]: 0.79-0.99); rs1041981 in the LTA gene (OR = 0.87, 95% CI: 0.78-0.98), and rs9344 in the CCND1 gene (OR = 1.14, 95% CI: 1.02-1.27), for those individuals carrying the rare allele. 19585495

2009

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Driven by findings that human papillomavirus (HPV)-induced degradation of p53 differs by a TP53 polymorphism at codon 72 (Pro72Arg), past studies of TP53 genetic variants and cervical cancer have focused on this nonsynonymous polymorphism, with mixed results. 19423538

2009

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The results indicated that the polymorphism in TP53 (rs1042522) might be associated with risk of cervical cancer development in HPV16 infected women. 23534750

2013

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The Arg variant of p53 Arg72Pro is associated with progression of SIL to cervical cancer only in the presence of HPV positivity. 23065429

2012

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Women carrying the p53 Arg72Pro or p53 Pro72Pro increased the risk of cervical carcinoma (ORs and 95% CIs being 3.74 (2.65-5.30), 2.23 (1.49-3.34)). 19576684

2010

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE We failed to confirm earlier reports of increased cervical cancer susceptibility in women who harbor the p53 P72R allele. 12142377

2002

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The present hospital-based retrospective cohort study aimed to evaluate the influence of <i>TP53</i> Arg72Pro (rs1042522) polymorphism in the clinical outcome of 260 Caucasian patients diagnosed with cervical cancer and treated with concomitant radiotherapy and chemotherapy. 29731921

2018

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The aim of the present study was to analyze the association of p53 codon72 (arginine/proline) polymorphism (rs1042522) and Murine Double Minute 2 (MDM2) SNP309 T/G (rs2279744) with the advancement of cervical cancer by using polymerase chain reaction-restriction fragment length polymorphism method followed by direct sequencing. 23210739

2013

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE To better understand the role of this polymorphism in cervical cancer etiology, we investigated the association between p53 R72P and cervical cancer risk in Chinese women from southern Han. 20193851

2010

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE A hundred HIV-infected women were examined for HPV detection and its genotypes, as well as the frequencies of the SNPs Arg72Pro and SNP309 and their associations with CC risk factors. 25181402

2015

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Combined analysis revealed that the genotypes of rs4938723 CT/CC and TP53 Arg72Pro CG/CC had an increased cervical cancer risk (OR = 2.21, 95 % CI = 1.38-3.53). 26619844

2016

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The p53 R72P polymorphism does not influence cervical cancer development in a Portuguese population: a study in exfoliated cervical cells. 18205229

2008

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE Genetic polymorphisms of p73 G4C14-to-A4T14 at exon 2 and p53 Arg72Pro and the risk of cervical cancer in Japanese. 15036661

2004

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE The aim of this Human Genome Epidemiology (HuGE) review and meta-analysis was to derive a more precise estimation of the association between p53 codon 72 polymorphism (Arg72Pro, rs1042522 G>C) and cervical cancer risk among Asians. 23244080

2012

dbSNP: rs1042522
rs1042522
0.100 GeneticVariation BEFREE These results suggest that a heterozygous TP53 Arg72Pro genotype may contribute to cervical cancer susceptibility. 21665181

2011

dbSNP: rs10426502
rs10426502
0.010 GeneticVariation BEFREE The stratified analysis showed that <i>TNFAIP8L1</i>-rs10426502, -rs1060555, and <i>FLT1</i>-rs9513111 were associated with a decreased risk of cervical cancer amongst people older than 43 years. 31289124

2019

dbSNP: rs1042725
rs1042725
0.010 GeneticVariation BEFREE The minor allele "C" of rs1042725 in HMGA2 was associated with an increased risk of CC in the allele, dominant and log-additive models. 27677077

2016

dbSNP: rs1045935
rs1045935
0.010 GeneticVariation BEFREE Analysis of the SNPs after stratification based on CC clinical stage and subtype revealed that rs1048512, rs6659346, rs217727, rs9931702, and rs9302648 were associated with CC risk in clinical stages I-II; rs2862833, rs2732044, rs1030389, and rs1045935 were associated with CC risk in clinical stages III-IV; and rs217727, rs9931702, and rs9302648 were associated with CC risk in squamous carcinomas. 27765929

2016

dbSNP: rs1047840
rs1047840
0.010 GeneticVariation BEFREE These findings indicate that the SNPs of EXO1 K589E may contribute to cervical cancer carcinogenesis in Chinese populations. 22146767

2012

dbSNP: rs1048512
rs1048512
0.010 GeneticVariation BEFREE Analysis of the SNPs after stratification based on CC clinical stage and subtype revealed that rs1048512, rs6659346, rs217727, rs9931702, and rs9302648 were associated with CC risk in clinical stages I-II; rs2862833, rs2732044, rs1030389, and rs1045935 were associated with CC risk in clinical stages III-IV; and rs217727, rs9931702, and rs9302648 were associated with CC risk in squamous carcinomas. 27765929

2016

dbSNP: rs1048638
rs1048638
CA9
0.010 GeneticVariation BEFREE In conclusion, the finding that the <i>CA9</i> </span>SNP rs1</span>048638 exerts its action through duplexes of the miR-34a and <i>CA9</i> 3'-UTRs and plays a vital role in cervical cancer in Taiwanese women may be applicable to translational medicine. 29100431

2017

dbSNP: rs104886003
rs104886003
0.020 GeneticVariation BEFREE The PIK3CA E542K and E545K mutations promote glycolysis and proliferation via induction of the β-catenin/SIRT3 signaling pathway in cervical cancer. 30547809

2018