RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.720 GeneticVariation BEFREE In the present study, we investigated whether the oncogenic RET mutants RET2A (C634R) and RET2B (M918T) were regulated by LRIG1, and the possible effects of LRIG1 expression in thyroid cancer were investigated in three different clinical cohorts and in a RET2B-driven mouse model of MTC. 29436694 2018
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.720 GeneticVariation BEFREE In present result, RET rs1799939, rs1800858 and rs74799832 polymorphisms might be the risk factors for TC. 26191299 2015
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Vandetanib in patients with locally advanced or metastatic medullary thyroid cancer: a randomized, double-blind phase III trial. 22025146 2012
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
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: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Targeted therapies for thyroid tumors. 21455200 2011
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR The effects of four different tyrosine kinase inhibitors on medullary and papillary thyroid cancer cells. 21470995 2011
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Phase II study of daily sunitinib in FDG-PET-positive, iodine-refractory differentiated thyroid cancer and metastatic medullary carcinoma of the thyroid with functional imaging correlation. 20847059 2010
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Vandetanib for the treatment of patients with locally advanced or metastatic hereditary medullary thyroid cancer. 20065189 2010
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Phase II clinical trial of sorafenib in metastatic medullary thyroid cancer. 20368568 2010
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Phase II trial of sorafenib in metastatic thyroid cancer. 19255327 2009
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Phase II trial of sorafenib in advanced thyroid cancer. 18541894 2008
dbSNP: rs74799832
rs74799832
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
C 0.720 CausalMutation CLINVAR Molecular biology of the MEN2 gene. 9681850 1998
dbSNP: rs77709286
rs77709286
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
G 0.700 GeneticVariation CLINVAR Vandetanib in patients with locally advanced or metastatic medullary thyroid cancer: a randomized, double-blind phase III trial. 22025146 2012
dbSNP: rs77709286
rs77709286
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
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: rs77709286
rs77709286
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
G 0.700 GeneticVariation CLINVAR The effects of four different tyrosine kinase inhibitors on medullary and papillary thyroid cancer cells. 21470995 2011
dbSNP: rs77709286
rs77709286
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
G 0.700 GeneticVariation CLINVAR Vandetanib for the treatment of patients with locally advanced or metastatic hereditary medullary thyroid cancer. 20065189 2010
dbSNP: rs1799939
rs1799939
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.020 GeneticVariation BEFREE In present result, RET rs1799939, rs1800858 and rs74799832 polymorphisms might be the risk factors for TC. 26191299 2015
dbSNP: rs1799939
rs1799939
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
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: rs75076352
rs75076352
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.010 GeneticVariation BEFREE In the present study, we investigated whether the oncogenic RET mutants RET2A (C634R) and RET2B (M918T) were regulated by LRIG1, and the possible effects of LRIG1 expression in thyroid cancer were investigated in three different clinical cohorts and in a RET2B-driven mouse model of MTC. 29436694 2018
dbSNP: rs1800858
rs1800858
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.010 GeneticVariation BEFREE In present result, RET rs1799939, rs1800858 and rs74799832 polymorphisms might be the risk factors for TC. 26191299 2015
dbSNP: rs75234356
rs75234356
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.010 GeneticVariation BEFREE Nevertheless, an extensive molecular analysis that included all codons was prompted by the diagnosis of thyroid neoplasm in a patient's sister, and identified the rare intracellular RET p.Ser891Ala mutation. 23295303 2012
dbSNP: rs377767414
rs377767414
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.010 GeneticVariation BEFREE If the germline RET R770Q variant has a causative role in the pathogenesis of the mixed medullar/follicular derived histology of the thyroid tumour in the index patient of family 1 has to be proven. 20013610 2010
dbSNP: rs377767427
rs377767427
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
0.010 GeneticVariation BEFREE New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour. 20013610 2010
dbSNP: rs79658334
rs79658334
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0040136
Disease:
Thyroid Neoplasm
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