Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE MTHFR C677T genetic polymorphism in combination with serum vitamin B<sub>2</sub>, B<sub>12</sub> and aberrant DNA methylation of P16 and P53 genes in esophageal squamous cell carcinoma and esophageal precancerous lesions: a case-control study. 31754346

2019

dbSNP: rs12435483
rs12435483
0.010 GeneticVariation BEFREE A significantly decreased risk of cervical precancerous lesions for the TC genotype of rs12435483 in the <i>TRAF3</i> gene (OR<sub>adjusted</sub> = 0.67, 95% CI, 0.45-0.98) was also found. 30463990

2019

dbSNP: rs6052130
rs6052130
0.010 GeneticVariation BEFREE Moreover, <i>MAVS</i> rs6052130-mutant individuals have an increased vulnerability to high-risk HPV-induced cervical precancerous lesions. 30463990

2019

dbSNP: rs78303930
rs78303930
NES
0.010 GeneticVariation BEFREE The present study comparatively analyzed serial autopsies of Japanese patients (n=2,206; males, 1,225; females, 981; median, 80.7 years old; range, 33-104 years old) with malignant tumors of whole organs, with respect to the clinical information, and 5 single nucleotide polymorphisms of the nestin gene. p.A1199P associated with pancreatic cancer (odds ratio, 4.4; 95% confidence interval, 1.9-10.0, P=0.001) while it did not associate with malignant neoplasms in other organs. p.A1199P did not associate with precancerous lesions of the pancreas. 30988821

2019

dbSNP: rs879253942
rs879253942
0.010 GeneticVariation BEFREE MTHFR C677T genetic polymorphism in combination with serum vitamin B<sub>2</sub>, B<sub>12</sub> and aberrant DNA methylation of P16 and P53 genes in esophageal squamous cell carcinoma and esophageal precancerous lesions: a case-control study. 31754346

2019

dbSNP: rs14035
rs14035
RAN
0.010 GeneticVariation BEFREE Five single nucleotide polymorphisms (SNPs), including Ran-GTP (<i>RAN</i>) rs14035, exportin-5 (<i>XPO5</i>) rs11077, <i>DICER1</i> rs3742330, <i>DICER1</i> rs13078, and <i>TARBP2</i> rs784567, were genotyped in a case-control study to estimate risk factors of cervical precancerous lesions. 29853562

2018

dbSNP: rs1966265
rs1966265
0.010 GeneticVariation BEFREE In conclusion, our study demonstrated that FGFR4 rs2011077 and rs1966265 are associated with the progression of cervical normal tissues to precancerous lesions in Taiwanese women. 28378614

2018

dbSNP: rs2011077
rs2011077
0.010 GeneticVariation BEFREE In conclusion, our study demonstrated that FGFR4 rs2011077 and rs1966265 are associated with the progression of cervical normal tissues to precancerous lesions in Taiwanese women. 28378614

2018

dbSNP: rs3742330
rs3742330
0.010 GeneticVariation BEFREE A two-factor (<i>DICER1</i> rs3742330 and human papillomavirus (HPV) infection) and two three-factor (model 1: rs3742330, passive smoking, and HPV infection; model 2: rs3742330, abortion history, and HPV infection) interaction models for cervical precancerous lesions were identified. 29853562

2018

dbSNP: rs7708357
rs7708357
0.010 GeneticVariation BEFREE Real-time polymerase chain reaction and genotyping were used to detect the genotype frequencies of 4 FGFR4 single-nucleotide polymorphisms (SNPs), rs351855 (C/T, Gly388Arg), rs2011077 (G/A), rs7708357 (G/A), and rs1966265 (Ile10Val), in 138 patients with invasive cancer, 89 with precancerous lesions of uterine cervix, and 335 normal controls. 28378614

2018

dbSNP: rs784567
rs784567
0.010 GeneticVariation BEFREE Five single nucleotide polymorphisms (SNPs), including Ran-GTP (<i>RAN</i>) rs14035, exportin-5 (<i>XPO5</i>) rs11077, <i>DICER1</i> rs3742330, <i>DICER1</i> rs13078, and <i>TARBP2</i> rs784567, were genotyped in a case-control study to estimate risk factors of cervical precancerous lesions. 29853562

2018

dbSNP: rs16970849
rs16970849
0.010 GeneticVariation BEFREE The aim of the study was to evaluate the association of two SNPs of EVER1/2 genes' region (rs2290907, rs16970849) and the FAS-670 polymorphism with the susceptibility to precancerous lesions and cervical cancer in a Greek population. 27899077

2016

dbSNP: rs2290907
rs2290907
0.010 GeneticVariation BEFREE The aim of the study was to evaluate the association of two SNPs of EVER1/2 genes' region (rs2290907, rs16970849) and the FAS-670 polymorphism with the susceptibility to precancerous lesions and cervical cancer in a Greek population. 27899077

2016

dbSNP: rs281432
rs281432
0.010 GeneticVariation BEFREE Compared to homozygous wild CC, heterozygous CG, homozygous mutant GG, or genotypes with CG/GG display increased risks or a tendency of precancerous lesions or invasive cancer with strong power in rs281432. 26377999

2016

dbSNP: rs3093030
rs3093030
0.010 GeneticVariation BEFREE The homozygotic mutant alleles TT in rs3093030 and homozygotic mutant alleles GG in rs5498 were associated with a higher risk of invasive cancer and precancerous lesions, respectively, but with lower power. 26377999

2016

dbSNP: rs311678
rs311678
0.010 GeneticVariation BEFREE In conclusion, our results indicate that the rs311678 polymorphism in the cGAS gene confers genetic susceptibility to cervical precancerous lesions. 27705945

2016

dbSNP: rs5498
rs5498
0.010 GeneticVariation BEFREE The homozygotic mutant alleles TT in rs3093030 and homozygotic mutant alleles GG in rs5498 were associated with a higher risk of invasive cancer and precancerous lesions, respectively, but with lower power. 26377999

2016

dbSNP: rs10759932
rs10759932
0.010 GeneticVariation BEFREE TLR4 rs10759932 TC and C carriers were associated with a lower risk in developing precancerous lesions in the stomach in a Chinese Han population. 24269697

2014

dbSNP: rs4986790
rs4986790
0.010 GeneticVariation BEFREE We observed that frequencies of TLR-4 Asp299Gly variants were comparable between patients and control subjects, and also between positive and negative groups of precancerous lesions in patients. 18082569

2007