Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2516448
rs2516448
0.720 GeneticVariation BEFREE The C allele of rs9272143 conferred protection against cervical cancer (odds ratio [OR] = 0.73, 95% confidence interval [CI] = 0.65-0.82; P = 1.6 × 10(-7)), which is associated with higher expression level of HLA-DRB1, whereas the T allele of rs2516448 increased the susceptibility to cervical cancer (OR = 1.33, 95% CI = 1.19-1.49; P = 5.8 × 10(-7)), with the same association shown with MICA-A5.1. 24403192

2014

dbSNP: rs2516448
rs2516448
0.720 GeneticVariation GWASCAT Three independent loci in the major histocompatibility complex (MHC) region at 6p21.3 were associated with cervical cancer: the first is adjacent to the MHC class I polypeptide-related sequence A gene (MICA) (rs2516448; OR = 1.42, 95% CI = 1.31 to 1.54; P = 1.6×10(-18)); the second is between HLA-DRB1 and HLA-DQA1 (rs9272143; OR = 0.67, 95% CI = 0.62 to 0.72; P = 9.3×10(-24)); and the third is at HLA-DPB2 (rs3117027; OR=1.25, 95% CI = 1.15 to 1.35; P = 4.9×10(-8)). 23482656

2013

dbSNP: rs2516448
rs2516448
0.720 GeneticVariation BEFREE The cGAS-STING pathway in innate immunity plays an important role in protecting against HPV infection.Chen et al. described that the rs2516448 SNP in the MHC locus may affect susceptibility to cervical cancer, a finding that we attempted to replicate in a Chinese population. 27705945

2016

dbSNP: rs9277952
rs9277952
0.720 GeneticVariation GWASCAT A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs9277952
rs9277952
0.720 GeneticVariation BEFREE No association was found with the two SNPs (rs4282438 or rs9277952) that were recently identified within the HLA-DP region in a cervical cancer GWAS in the Chinese population. 24743517

2014

dbSNP: rs9277952
rs9277952
0.720 GeneticVariation BEFREE In this study, associations between invasive cervical cancer and four cervical cancer susceptibility loci (rs13117307 at 4q12, rs8067378 at 17q12, and rs4282438 and rs9277952 at 6p21.32) in the Han Chinese population were investigated in a Japanese population. 27193219

2016

dbSNP: rs8067378
rs8067378
0.710 GeneticVariation BEFREE In this study, associations between invasive cervical cancer and four cervical cancer susceptibility loci (rs13117307 at 4q12, rs8067378 at 17q12, and rs4282438 and rs9277952 at 6p21.32) in the Han Chinese population were investigated in a Japanese population. 27193219

2016

dbSNP: rs8067378
rs8067378
G 0.710 GeneticVariation GWASCAT We identified strong evidence of associations between cervical cancer and two new loci: 4q12 (rs13117307, Pcombined, stringently matched=9.69×10(-9), per-allele odds ratio (OR)stringently matched=1.26) and 17q12 (rs8067378, Pcombined, stringently matched=2.00×10(-8), per-allele ORstringently matched=1.18). 23817570

2013

dbSNP: rs3132461
rs3132461
G 0.700 GeneticVariation GWASCAT Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. 28806749

2017

dbSNP: rs6812281
rs6812281
T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies four SNPs associated with response to platinum-based neoadjuvant chemotherapy for cervical cancer. 28120872

2017

dbSNP: rs73730372
rs73730372
0.700 GeneticVariation GWASCAT Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus. 27285765

2016

dbSNP: rs9532669
rs9532669
A 0.700 GeneticVariation GWASCAT Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. 28806749

2017

dbSNP: rs1195571
rs1195571
0.010 GeneticVariation BEFREE For the individuals older than 43, rs4604006 (VEGF-C) was related to an increased cervical cancer risk under codominant model (p = .035), and rs12646659 was significantly associated with a reduced cervical cancer risk in allele, dominant, log-additive models (allele: p = .028; codominant: p = .037; log-additive: p = .037) However, there were no significant correlation of rs1000611 (VEGFR-2) and rs1195571 (VEGFR-3) with cervical cancer risk in Chinese Uygur population. 31478352

2019

dbSNP: rs180082
rs180082
0.010 GeneticVariation BEFREE This meta-analysis has shown that there is a lack of association of the Fas rs180082 polymorphisms with cervical cancer susceptibility. 23865866

2013

dbSNP: rs2808630
rs2808630
0.010 GeneticVariation BEFREE The four most common single nucleotide gene polymorphisms CRP1919 (rs1417938), CRP2667 (rs1800947), CRP3872 (rs1205), and CRP5237 (rs2808630) were evaluated in 178 patients with cervical cancer. 21737650

2011

dbSNP: rs2844511
rs2844511
0.010 GeneticVariation BEFREE A statistically significant association was observed between single nucleotide polymorphism (SNP) CHR6 rs2844511 and CC risk: the OR for carriers of the GA or GG genotypes was 0.70 (95% CI: 0.43-1.14) and 0.61 (95% CI: 0.38-0.98), respectively, relative to carriers of AA genotype (p-value for trend 0.03). 28505207

2017

dbSNP: rs4769793
rs4769793
0.010 GeneticVariation BEFREE Collectively, these findings suggested that STAT3 gene polymorphism (rs4769793) was associated with the susceptibility as well as poor differentiation and parametrial invasion of cervical cancer in Chinese women. 21668356

2011

dbSNP: rs6457617
rs6457617
0.010 GeneticVariation BEFREE Persistent HPV16/18 infection in Indian women with the A-allele (rs6457617) of HLA-DQB1 and T-allele (rs16944) of IL-1β -511 is associated with development of cervical carcinoma. 25893807

2015

dbSNP: rs1800682
rs1800682
0.020 GeneticVariation BEFREE Subgroup analysis by ethnicity suggested that there was no association between CD95 rs1800682 p</span>olymorphism and cervical cancer risk in Asians, Caucasians, and Africans. 24114012

2014

dbSNP: rs1800682
rs1800682
0.020 GeneticVariation BEFREE However, we did not observe any association between the cervical cancer risk and the rs2234767 and rs1800682 polymorphisms. 27790710

2017

dbSNP: rs2234767
rs2234767
0.010 GeneticVariation BEFREE However, we did not observe any association between the cervical cancer risk and the rs2234767 and rs1800682 polymorphisms. 27790710

2017

dbSNP: rs59661306
rs59661306
G 0.700 GeneticVariation GWASCAT Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. 30412241

2019

dbSNP: rs1800624
rs1800624
0.010 GeneticVariation BEFREE In conclusion, RAGE SNPs rs1800624 was associated with some clinicopathological variables in cervical cancer. 30410591

2018

dbSNP: rs9302648
rs9302648
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: rs9931702
rs9931702
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