Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886037822
rs886037822
CDH1
A 0.700 CausalMutation CLINVAR A novel mutation in the CDH1 gene in a Spanish family with hereditary diffuse gastric cancer. 27512640

2016
dbSNP: rs886037822
rs886037822
CDH1
A 0.700 CausalMutation CLINVAR Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. 25741868

2015