Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Panel testing reveals nonsense and missense CDH1 mutations in families without hereditary diffuse gastric cancer. 27064202

2016
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer. 27153395

2016
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Hereditary diffuse gastric cancer: translation of CDH1 germline mutations into clinical practice. 20373070

2010
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Mechanisms and sequelae of E-cadherin silencing in hereditary diffuse gastric cancer. 18788075

2008
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Hereditary diffuse gastric cancer: association with lobular breast cancer. 18046629

2008
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria. 15235021

2004
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Novel germline CDH1 mutations in hereditary diffuse gastric cancer families. 11968084

2002