| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.700 | CausalMutation | CLINVAR | Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers. | 28946813 | 2017 |
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|
T | 0.700 | CausalMutation | CLINVAR | Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation. | 27673361 | 2016 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation. | 27673361 | 2016 |
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|
T | 0.700 | CausalMutation | CLINVAR | Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients. | 26269449 | 2015 |
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|
T | 0.700 | CausalMutation | CLINVAR | Overexpression of genes involved in miRNA biogenesis in medullary thyroid carcinomas with RET mutation. | 24569963 | 2014 |
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|
T | 0.700 | CausalMutation | CLINVAR | A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma. | 25319874 | 2014 |
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|
T | 0.700 | CausalMutation | CLINVAR | Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism. | 21690267 | 2011 |
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|
T | 0.700 | CausalMutation | CLINVAR | Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family. | 21678021 | 2011 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro. | 20103606 | 2010 |
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|
T | 0.700 | CausalMutation | CLINVAR | Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro. | 20103606 | 2010 |
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|
T | 0.700 | CausalMutation | CLINVAR | Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases. | 15858153 | 2005 |