Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs929783669
rs929783669
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 GeneticVariation UNIPROT

dbSNP: rs121913483
rs121913483
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 GeneticVariation UNIPROT

dbSNP: rs1058808
rs1058808
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 GeneticVariation BEFREE <b>Conclusions:</b> Our results suggested that the combination of <i>HER2</i> rs1136201and rs1058808 was significantly associated with the susceptibility of CCa. 30719131

2019

dbSNP: rs9277535
rs9277535
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 GeneticVariation BEFREE <i>Conclusion.</i> HLA-DP gene polymorphisms (HLA-DPB1⁎03:01, DPB1⁎04:02, DPB1⁎13:01, rs9277535, and rs3117027) were significantly associated with cervical cancer. 30009173

2018

dbSNP: rs3117027
rs3117027
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 GeneticVariation BEFREE <i>Conclusion.</i> HLA-DP gene polymorphisms (HLA-DPB1⁎03:01, DPB1⁎04:02, DPB1⁎13:01, rs9277535, and rs3117027) were significantly associated with cervical cancer. 30009173

2018

dbSNP: rs1048943
rs1048943
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.090 GeneticVariation BEFREE (2) rs1048943 (CYP1A1 A4889G) showed the strongest association with cervical cancer in the allele effect model (1.83[1.57, 2.13]); in addition, rs1048943 (CYP1A1 A4889G) had a very strong association in the dominant and recessive effect model. 25928231

2015

dbSNP: rs1217691063
rs1217691063
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.100 GeneticVariation BEFREE Cervical cancer with polymorphism in MTHFR C677T gene: a systematic review and meta-analysis. 23070908

2013

dbSNP: rs1217691063
rs1217691063
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.100 GeneticVariation BEFREE C677T polymorphism of MTHFR gene may increase the risk of cervical cancer in the complete over-dominant model. 23490201

2013

dbSNP: rs4646903
rs4646903
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.050 GeneticVariation BEFREE rs4646903 minor alleles and interaction between rs4646903 and rs1048943 were associated with increased cervical cancer risk. 27265845

2016

dbSNP: rs1292037
rs1292037
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 GeneticVariation BEFREE In addition to that, the G allele at rs1292037 (A > G) locus increases the risk of preoperative chemoresistance to cisplatin plus paclitaxel and is a poor prognostic factor for patients with CC. 30447706

2018

dbSNP: rs9277952
rs9277952
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.720 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs9277535
rs9277535
CUI: C4048328
Disease: cervical cancer
cervical cancer
A 0.720 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs9391756
rs9391756
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs7770370
rs7770370
CUI: C4048328
Disease: cervical cancer
cervical cancer
A 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs4713607
rs4713607
CUI: C4048328
Disease: cervical cancer
cervical cancer
A 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs3129275
rs3129275
CUI: C4048328
Disease: cervical cancer
cervical cancer
A 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs3117039
rs3117039
CUI: C4048328
Disease: cervical cancer
cervical cancer
A 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs3117008
rs3117008
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs213210
rs213210
CUI: C4048328
Disease: cervical cancer
cervical cancer
T 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs2116260
rs2116260
CUI: C4048328
Disease: cervical cancer
cervical cancer
T 0.700 GeneticVariation GWASDB A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. 23817570

2013

dbSNP: rs3918242
rs3918242
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 GeneticVariation BEFREE A hospital-based case-control study was conducted in 230 patients with cervical cancer and 230 healthy controls to investigate the possible association between the MMP2 rs243865, MMP3 rs3025058, MMP7 rs11568818, and MMP9 rs3918242 polymorphisms, respectively, and the risk of cervical cancer. 26526578

2016

dbSNP: rs878854066
rs878854066
CUI: C4048328
Disease: cervical cancer
cervical cancer
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: rs1131691014
rs1131691014
CUI: C4048328
Disease: cervical cancer
cervical cancer
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
CUI: C4048328
Disease: cervical cancer
cervical cancer
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: rs1353702185
rs1353702185
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 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