rs1555515731, CDH1

N. diseases: 4
Source: CURATED ×
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 Characterization of a recurrent germ line mutation of the E-cadherin gene: implications for genetic testing and clinical management. 16061854 2005
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
0.700 CausalMutation CLINVAR
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
0.700 CausalMutation CLINVAR
Hereditary Diffuse Gastric Cancer
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
0.700 CausalMutation CLINVAR