Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE In addition, we found an increased risk of cancer in both rs2736098 and rs401681 homozygous variant genetic model. 23707794

2013

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE The A allele in the rs2736098 G > A polymorphism contributes to susceptibility in many types of cancer, especially lung cancer and bladder cancer. 29695979

2018

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE These findings provided further evidence that TERT rs2736098 variant may modify the susceptibility to cancer. 27273963

2016

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE Additionally, rs2736098 (p-valuecor ≤ 0.0234) was associated with only sporadic cancers; also in group without carriers of high-risk mutation. 24171766

2013

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE Our meta-analysis did not show that the TERT rs2736098 plays an important role in cancer risk. 23244087

2012

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE <i>TERT</i> rs2736098 (Ex2-659G>A) polymorphism and cancer susceptibility: evidence from a comprehensive meta-analysis. 29221218

2017

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE In addition, single nucleotide polymorphisms (SNPs) in the TERT rs2736098 and rs2736100 are significantly associated with cancer susceptibility. 28416747

2017

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE Single-nucleotide polymorphisms (SNPs) of TERT-rs2736098 (C > T) and CLPTM1L-rs401681(C > T) at the 5p15.33 locus are significantly associated with cancer risk as reported in genome-wide association studies (GWAS), but there are no reported studies for squamous cell carcinoma of the head and neck (SCCHN). 20802237

2010

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE In the meta-analysis, a borderline significant association between the rs2736098 polymorphism and overall cancer risk was observed (AA vs. GG: OR = 1.25, 95% CI = 1.07-1.46; AA vs. AG+GG: OR = 1.22, 95% CI = 1.06-1.41; additive model: OR = 1.10, 95% CI = 1.02-1.18), and further stratifications demonstrated a moderately increased risk for lung and bladder cancer, Asian ethnicity and hospital-based studies. 24260099

2013

dbSNP: rs2736098
rs2736098
0.100 GeneticVariation BEFREE Overall, this meta-analysis indicates that the TERT rs2736098 polymorphism may have little involvement in cancer susceptibility. 22994782

2012

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE We genotyped telomerase reverse transcriptase (TERT) rs2736100 variants, the SNP associated with a risk of multiple-types of cancer, in patients with UTUC (n = 212) and evaluated the relationship between the rs2736100 and UTUC risk by comparing to 289 healthy controls. 26934125

2016

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE Increased cancer risk was found between TERT-rs2736100, as well as CLPTM1L-rs402710 and cancer susceptibility. 23707794

2013

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE In all genetic models, the association between the TERT rs2736100 polymorphism and cancer risk was significant. 22221621

2012

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE The TERT rs2736100 polymorphism was associated with increased overall cancer risk in five genetic models [homozygous model (GG vs. TT): odds ratio (OR) = 1.39, 95% confidence interval (95% CI) = 1.26-1.54, P < 0.001; heterozygous model (TG vs. TT): OR = 1.16, 95% CI = 1.11-1.23, P < 0.001; dominant model (TG + GG vs. TT): OR = 1.23, 95% CI = 1.15-1.31, P < 0.001; recessive model (GG vs. TG + TT): OR = 1.25, 95% CI = 1.16-1.35, P < 0.001; and allele contrast model (G vs. T): OR = 1.17, 95% CI = 1.12-1.23, P < 0.001]. 28418878

2017

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE The rs2736100 association demonstrates an influence of variation at 5p15.33 on CRC risk and further evidence that the 5p15.33 (TERT-CLPTM1L) locus has pleiotropic effects (reflecting generic or lineage-specific effects) on cancer risk. 22878375

2012

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE Telomerase Reverse Transcriptase Polymorphism rs2736100: A Balancing Act between Cancer and Non-Cancer Disease, a Meta-Analysis. 29536006

2018

dbSNP: rs2736100
rs2736100
0.070 GeneticVariation BEFREE For rs2736100, the cancer risk genotype CC was significantly associated with a reduced incidence of TERT promoter mutations compared to AA + AC variants [Odds ratio (OR): 0.181, 95% Confidence interval (CI): 0.0543-0.601, P = 0.004]. 28416747

2017

dbSNP: rs2853669
rs2853669
0.040 GeneticVariation BEFREE However, we identified a modifying effect of rs2853669 on <i>TERTp</i> mutations in that, among cancer patients with <i>TERTp</i> mutations, only those carrying the TT genotype had a poor survival (Hazard ratio = 1.56, 95% confidence interval = 1.06-2.28); subgroup analyses by cancer type also supported these results. 28881610

2017

dbSNP: rs2853669
rs2853669
0.040 GeneticVariation BEFREE The results of this meta-analysis suggest that the TERT rs2853669 polymorphism is associated with a significantly increased risk of cancer, particularly lung cancer, in Asian populations. 29534075

2018

dbSNP: rs2853669
rs2853669
0.040 GeneticVariation BEFREE We observed an association of allele rs2853669 C with increased risk of prostate cancer (co-dominant model TC vs. TT OR = 1.65, P = 0.002; additive model OR = 1.42, P = 0.005; dominant model: OR = 1.64, P = 0.001) and allele rs7726159 A with reduced risk of this malignancy (сo-dominant model: AA vs. CC OR = 0.42, P = 0.002; additive model: OR = 0.69, P = 0.002; dominant model: OR = 0.67, P = 0.01; recessive model: OR = 0.48, P = 0.005). 25296732

2015

dbSNP: rs2853669
rs2853669
0.040 GeneticVariation BEFREE A common single-nucleotide polymorphism in the telomerase reverse transcriptase (TERT) promoter, rs2853669 influences patient survival rates and the risk of developing cancer. 26575952

2016

dbSNP: rs10069690
rs10069690
0.020 GeneticVariation BEFREE The cancer risk alleles of rs2242652 and rs1006</span>9690, respectively, increase silencing and generate a truncated TERT splice variant. 23535731

2013

dbSNP: rs10069690
rs10069690
0.020 GeneticVariation BEFREE This meta-analysis suggested that the TERT rs10069690 polymorphism may be a risk factor for cancer, especially breast cancer, ovarian cancer, lung cancer, thyroid cancer, and RCC. 31454181

2019

dbSNP: rs2853676
rs2853676
0.020 GeneticVariation BEFREE Mean RTL at age 60 was associated with four genetic variants of the hTERT gene (rs2736100, rs2853672, rs2853677, and rs2853676), two of which reported to be associated with cancer risk. 22539396

2012

dbSNP: rs2853676
rs2853676
0.020 GeneticVariation BEFREE A significant association between TERT rs2853676 allele A and cancer susceptibility was demonstrated under a per-allele risk analysis (OR = 1.08, 95% CI = 1.04-1.13). 26042809

2015