Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587783047
rs587783047
CDH1
T 0.700 CausalMutation CLINVAR Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome. 24493355

2014
dbSNP: rs587783047
rs587783047
CDH1
T 0.700 CausalMutation CLINVAR CDH1-related hereditary diffuse gastric cancer syndrome: clinical variations and implications for counseling. 22020549

2012
dbSNP: rs587783047
rs587783047
CDH1
T 0.700 CausalMutation CLINVAR Identification of germ-line E-cadherin mutations in gastric cancer families of European origin. 9751616

1998