Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE <i>BRAF</i> V600E mutations have been successfully treated with targeted therapy in melanoma, non-small cell lung cancer, and thyroid cancer. 29295876

2018

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE <i>BRAF</i> V600E mutations have been successfully treated with targeted therapy in melanoma, non-small cell lung cancer, and thyroid cancer. 29295876

2018

dbSNP: rs74799832
rs74799832
RET
C 0.720 CausalMutation CLINVAR Thyroid cancer cell lines harboring RET/PTC1 (TPC-1), RET M918T (MZ-CRC1) and RET C634W (TT) alterations, as well as TPC-1 xenografts, were treated with JAK inhibitor, AZD1480. 23056499

2012

dbSNP: rs77709286
rs77709286
RET
G 0.700 GeneticVariation CLINVAR Thyroid cancer cell lines harboring RET/PTC1 (TPC-1), RET M918T (MZ-CRC1) and RET C634W (TT) alterations, as well as TPC-1 xenografts, were treated with JAK inhibitor, AZD1480. 23056499

2012

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Thyroid neoplasms with PD-L1 expression also ae enriched with BRAF V600E mutations, suggesting that they are associated with more aggressive behavior. 31821747

2020

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Thyroid neoplasms with PD-L1 expression also ae enriched with BRAF V600E mutations, suggesting that they are associated with more aggressive behavior. 31821747

2020

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE Hence, recent research efforts have been performed trying to explore several inhibitors of the V600E mutation-containing BRAF kinase as potential therapeutic options in thyroid cancer refractory to standard interventions. 30481266

2019

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE Hence, recent research efforts have been performed trying to explore several inhibitors of the V600E mutation-containing BRAF kinase as potential therapeutic options in thyroid cancer refractory to standard interventions. 30481266

2019

dbSNP: rs1799939
rs1799939
RET
0.020 GeneticVariation BEFREE A G691S RET polymorphism was present with a higher frequency in radiation-induced epithelial thyroid tumours (55%) than in sporadic tumours (20%) and in control normal thyroid tissues (15%). 12085189

2002

dbSNP: rs147394161
rs147394161
0.010 GeneticVariation BEFREE A genetic polymorphism, Y609C, was seen in 7% of thyroid tumors but was not related to gene downregulation. 20124489

2010

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE A literature search using PubMed identified all the pertinent literature on the identification and utilization of the B-Raf(V600E) mutation in thyroid cancer. 20637346

2010

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE A literature search using PubMed identified all the pertinent literature on the identification and utilization of the B-Raf(V600E) mutation in thyroid cancer. 20637346

2010

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE A missense mutation was found at T1796A (V599E) in exon 15 in four of the six cell lines and 51 of 207 thyroid tumors (24.6%; 0 of 20 follicular adenoma, 0 of 11 follicular carcinoma, 49 of 170 papillary carcinomas, and 2 of 6 undifferentiated carcinomas). 12970315

2003

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE A missense mutation was found at T1796A (V599E) in exon 15 in four of the six cell lines and 51 of 207 thyroid tumors (24.6%; 0 of 20 follicular adenoma, 0 of 11 follicular carcinoma, 49 of 170 papillary carcinomas, and 2 of 6 undifferentiated carcinomas). 12970315

2003

dbSNP: rs10069690
rs10069690
0.020 GeneticVariation BEFREE A previous genome-wide association study showed that hTERT rs10069690 and rs2736100 polymorphisms were associated with thyroid cancer risk. 31538903

2019

dbSNP: rs2736100
rs2736100
0.020 GeneticVariation BEFREE A previous genome-wide association study showed that hTERT rs10069690 and rs2736100 polymorphisms were associated with thyroid cancer risk. 31538903

2019

dbSNP: rs79658334
rs79658334
RET
0.010 GeneticVariation BEFREE A rapid method for the purification of wild-type and V804M mutant ret catalytic domain: A tool to study thyroid cancer. 16490247

2006

dbSNP: rs2145418
rs2145418
0.010 GeneticVariation BEFREE A statistically significant association between thyroid cancer incidence and the rs2145418 and rs4658973 polymorphisms was found (P < 0.0001). 18559567

2008

dbSNP: rs4658973
rs4658973
0.010 GeneticVariation BEFREE A statistically significant association between thyroid cancer incidence and the rs2145418 and rs4658973 polymorphisms was found (P < 0.0001). 18559567

2008

dbSNP: rs17879961
rs17879961
0.020 GeneticVariation BEFREE A truncating mutation (IVS2 + 1G>A, 1100delC or del5395) was associated with a higher risk of thyroid cancer (OR = 5.7; p = 0.006), than was the missense mutation I157T (OR = 2.8; p = 0.0001). 25583358

2015

dbSNP: rs778212685
rs778212685
0.010 GeneticVariation BEFREE A truncating mutation (IVS2 + 1G>A, 1100delC or del5395) was associated with a higher risk of thyroid cancer (OR = 5.7; p = 0.006), than was the missense mutation I157T (OR = 2.8; p = 0.0001). 25583358

2015

dbSNP: rs786203472
rs786203472
0.010 GeneticVariation BEFREE A truncating mutation (IVS2 + 1G>A, 1100delC or del5395) was associated with a higher risk of thyroid cancer (OR = 5.7; p = 0.006), than was the missense mutation I157T (OR = 2.8; p = 0.0001). 25583358

2015

dbSNP: rs863224748
rs863224748
0.010 GeneticVariation BEFREE A truncating mutation (IVS2 + 1G>A, 1100delC or del5395) was associated with a higher risk of thyroid cancer (OR = 5.7; p = 0.006), than was the missense mutation I157T (OR = 2.8; p = 0.0001). 25583358

2015

dbSNP: rs113488022
rs113488022
0.100 GeneticVariation BEFREE According to our experimental results, the panel including cf-DNA, SLC5A8 and SLC26A4 hypermethylation, and BRAF(V600E) analysis appears easy, reproducible, and non-invasive for the diagnosis on TC. 23931930

2013

dbSNP: rs121913377
rs121913377
0.100 GeneticVariation BEFREE According to our experimental results, the panel including cf-DNA, SLC5A8 and SLC26A4 hypermethylation, and BRAF(V600E) analysis appears easy, reproducible, and non-invasive for the diagnosis on TC. 23931930

2013