rs876658261, CDH1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.700 CausalMutation CLINVAR E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer. 10477433 1999
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer. 10477433 1999