rs587781290, CDH1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. 25186627 2015
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment. 26270727 2015
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment. 26270727 2015
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289 2014
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR Germline E-cadherin mutations in familial lobular breast cancer. 17660459 2007
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR Germline E-cadherin mutations in familial lobular breast cancer. 17660459 2007