Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10136427
rs10136427
0.010 GeneticVariation BEFREE Only the associations between rs10136427 and rs7267944 and DTC risk were replicated in the Polish and the Spanish populations with little evidence of population heterogeneity (GWAS and all replications combined, OR = 1.30, P = 9.30 × 10(-7) and OR = 1.32, P = 1.34 × 10(-8), respectively). 25029422

2014

dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE Significant association of TP53 Arg72Pro polymorphism in susceptibility to differentiated thyroid cancer. 25835179

2015

dbSNP: rs1042522
rs1042522
0.020 GeneticVariation BEFREE Thus, in this study, we analyzed the associations of intron 3 Ins16bp and exon 4 Arg72Pro polymorphisms, as well as their combined genotypes and haplotypes with the risk of differentiated thyroid carcinoma in Iranian-Azeri patients. 25410025

2015

dbSNP: rs1057519695
rs1057519695
0.010 GeneticVariation BEFREE BRAF mutation was present in 65% of 94 DTC and p.Q61R NRAS in one. 24468978

2014

dbSNP: rs1057519834
rs1057519834
0.010 GeneticVariation BEFREE BRAF mutation was present in 65% of 94 DTC and p.Q61R NRAS in one. 24468978

2014

dbSNP: rs10741657
rs10741657
0.010 GeneticVariation BEFREE German patients (n=253) with DTC (papillary thyroid carcinoma [PTC] and follicular thyroid carcinoma [FTC]) and HC (n=302) were genotyped for polymorphisms within the vitamin D metabolizing enzymes such as 25-hydroxylase (CYP2R1[rs12794714, rs10741657]), 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1[rs10877012, rs4646536]), and 25-hydroxyvitamin D 24-hydrolase (CYP24A1[rs927650, rs2248137, rs2296241]). 22690899

2012

dbSNP: rs10808556
rs10808556
0.010 GeneticVariation BEFREE The polymorphisms rs10808556 and rs1447295 showed an association with the risk of DTC (the strongest were the heterozygotes with OR, 1.38; 95% CI, 1.13-1.68 and OR, 1.35; 95% CI, 1.02-1.78, respectively), but, overall, they were unable to reach the statistically significant threshold following Bonferroni's correction. 24008490

2013

dbSNP: rs10877012
rs10877012
0.010 GeneticVariation BEFREE German patients (n=253) with DTC (papillary thyroid carcinoma [PTC] and follicular thyroid carcinoma [FTC]) and HC (n=302) were genotyped for polymorphisms within the vitamin D metabolizing enzymes such as 25-hydroxylase (CYP2R1[rs12794714, rs10741657]), 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1[rs10877012, rs4646536]), and 25-hydroxyvitamin D 24-hydrolase (CYP24A1[rs927650, rs2248137, rs2296241]). 22690899

2012

dbSNP: rs11175834
rs11175834
T 0.700 GeneticVariation GWASCAT Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. 28703219

2017

dbSNP: rs11214077
rs11214077
0.010 GeneticVariation BEFREE Our current study shows that SDHD-G12S and -H50R variants cause down-regulation of autophagy, demonstrating a role for SDHD in autophagy-associated pathogenesis of differentiated thyroid cancer. 28164237

2017

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE Thus, in this study, we analyzed the associations of intron 3 Ins16bp and exon 4 Arg72Pro polymorphisms, as well as their combined genotypes and haplotypes with the risk of differentiated thyroid carcinoma in Iranian-Azeri patients. 25410025

2015

dbSNP: rs1131691014
rs1131691014
0.020 GeneticVariation BEFREE Significant association of TP53 Arg72Pro polymorphism in susceptibility to differentiated thyroid cancer. 25835179

2015

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE BRAF V600E Status and Stimulated Thyroglobulin at Ablation Time Increase Prognostic Value of American Thyroid Association Classification Systems for Persistent Disease in Differentiated Thyroid Carcinoma. 31093278

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE These data suggest that BRAF(V600E)-mutated DTCs are significantly more (18)F-FDG-avid than BRAF-WT tumors. 25814520

2015

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Neither the presence of V600E BRAF mutations nor that of a well-differentiated thyroid carcinoma changed the outcome or disease-free survival. 24777145

2014

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE DTC was present in half of the cases.BRAF V600E mutation was identified in nine of 36 (25%) ATCs; seven cases had identical mutations in both the ATC and DTC components. 17989125

2008

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Role of B-Raf(V600E) in differentiated thyroid cancer and preclinical validation of compounds against B-Raf(V600E). 19356676

2009

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Our results show a high rate and a strong prognostic role of the classical BRAF (V600E) mutation and also suggest a common occurrence of non-hot spot mutations in adult DTC from this highly inbred population. 27387551

2016

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE This study investigated the role of molecular studies in preoperative diagnosis of DTC and</span> the association of p.V600E mutation with prognostic factors. 24468978

2014

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE We found TERT promoter mutations in 0.0% (0/179) of benign thyroid nodules and 7.0% (9/129) of thyroid nodules of differentiated thyroid cancer, representing a 100% diagnostic specificity and 7.0% sensitivity, with the latter rising to 38.0% (49/129) when combined with BRAF V600E testing. 25121551

2014

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The genetic duet of BRAF V600E/RAS and TERT promoter mutations is a most robust prognostic genetic pattern for poor prognosis of differentiated thyroid cancer. 30717896

2019

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE The aims of this study were to evaluate the utility of US-guided FNAB in the diagnostic assessment of nodules with or without clinical/US features suggestive for malignancy and to investigate the additional contribution of BRAF V600E mutation analysis in the detection of differentiated thyroid cancer. 22535974

2012

dbSNP: rs11554290
rs11554290
0.010 GeneticVariation BEFREE BRAF mutation was present in 65% of 94 DTC and p.Q61R NRAS in one. 24468978

2014

dbSNP: rs116909374
rs116909374
0.020 GeneticVariation BEFREE Among Europeans, we found that the two SNPs previously reported at 9q22 were not independently associated to DTC and that rs965513 was the predominant signal; at 14q13, we showed that the haplotype rs944289[C]-rs116909374[C]-rs999460[T] was significantly associated with DTC risk and that the association with rs116909374 differed by smoking status (p-interaction = 0.03). 26991144

2016

dbSNP: rs116909374
rs116909374
0.020 GeneticVariation BEFREE Five germline genetic variants (rs116909374, rs965513, rs944289, rs966423, and rs2439302) have been associated in genome-wide association studies (GWAS) with increased risk of differentiated thyroid cancer (DTC), but their role in mortality of patients has not been established. 26490305

2016