Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs59661306
rs59661306
ADGRV1 ; LUCAT1
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: rs6547598
rs6547598
TCF7L1
A 0.700 GeneticVariation GWASCAT Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. 30412241

2019
dbSNP: rs7457728
rs7457728
LINC01445
C 0.700 GeneticVariation GWASCAT Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. 30412241

2019
dbSNP: rs3132461
rs3132461 		G 0.700 GeneticVariation GWASCAT Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. 28806749

2017
dbSNP: rs4396968
rs4396968
GABRB1
T 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: rs9532669
rs9532669 		A 0.700 GeneticVariation GWASCAT Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. 28806749

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: rs997363
rs997363
C2orf83
C 0.700 GeneticVariation GWASCAT Genome-wide association study of HPV-associated cervical cancer in Japanese women. 24700089

2014
dbSNP: rs121913105
rs121913105
FGFR3
C 0.700 CausalMutation CLINVAR

dbSNP: rs121913482
rs121913482
FGFR3
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913483
rs121913483
FGFR3
G 0.700 CausalMutation CLINVAR

dbSNP: rs28931614
rs28931614
FGFR3
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933068
rs28933068
FGFR3
G 0.700 CausalMutation CLINVAR

dbSNP: rs28934571
rs28934571
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs4647924
rs4647924
FGFR3
G 0.700 CausalMutation CLINVAR

dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE MTHFR C677T polymorphism was not associated with cervical cancer and HPV infection. 31170928

2019
dbSNP: rs25487
rs25487
XRCC1
0.100 GeneticVariation BEFREE We also observed that the rs25487 mutation was significantly increased within the cervical cancer</span> population. 30616520

2019
dbSNP: rs1042522
rs1042522
TP53
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: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE However, the MTHFR C677T polymorphism was not associated with the risk of cervical cancer or CIN. 29740106

2018
dbSNP: rs25487
rs25487
XRCC1
0.100 GeneticVariation BEFREE In view of the exiting heterogeneity, we did subgroup analysis stratified</span> by ethnicity, resulting in the fact that the Arg39</span>9Gln polymorphism was related to the decreased risk of cervical cancer. 27903984

2017
dbSNP: rs25487
rs25487
XRCC1
0.100 GeneticVariation BEFREE This meta-analysis showed that the XRCC1 Arg399Gln GA variant might be risk alleles for cervical cancer susceptibility in the Chinese population, and further studies in other ethnic groups are required to arrive at definite conclusions. 27487002

2017
dbSNP: rs1042522
rs1042522
TP53
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: rs1131691014
rs1131691014
TP53
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: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE This study indicated that the MTHFR C677T may be no associated with cervical cancer risk, and yet the MTHFR A1298C polymorphism may be a risk factor for cervical cancer. 26879954

2016