Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines. 25452455 2015
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline. 22167527 2012
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies. 17440981 2007
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. 15604628 2004
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT The interaction of DNA mismatch repair proteins with human exonuclease I. 11427529 2001
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 GeneticVariation UNIPROT The molecular basis of Turcot's syndrome. 7661930 1995
Turcot syndrome (disorder)
CUI: C0265325
Disease: Turcot syndrome (disorder)
0.800 CausalMutation CLINVAR
Hereditary Non-Polyposis Colon Cancer Type 2
CUI: C1333991
Disease: Hereditary Non-Polyposis Colon Cancer Type 2
0.700 CausalMutation CLINVAR
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
0.700 CausalMutation CLINVAR