Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776398
rs587776398
CDH1
G 0.700 CausalMutation CLINVAR CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS). 27192129

2016
dbSNP: rs587780113
rs587780113
CDH1
A 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: rs587780113
rs587780113
CDH1
A 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs587780113
rs587780113
CDH1
A 0.700 CausalMutation CLINVAR Panel testing reveals nonsense and missense CDH1 mutations in families without hereditary diffuse gastric cancer. 27064202

2016
dbSNP: rs587780113
rs587780113
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: rs587780113
rs587780113
CDH1
C 0.700 CausalMutation CLINVAR Panel testing reveals nonsense and missense CDH1 mutations in families without hereditary diffuse gastric cancer. 27064202

2016
dbSNP: rs587780113
rs587780113
CDH1
T 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: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Roles for E-cadherin cell surface regulation in cancer. 27582386

2016
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104

2016
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Roles for E-cadherin cell surface regulation in cancer. 27582386

2016
dbSNP: rs587783050
rs587783050
CDH1
A 0.700 CausalMutation CLINVAR Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients. 27995193

2016
dbSNP: rs587783050
rs587783050
CDH1
A 0.700 CausalMutation CLINVAR Prophylactic total gastrectomy in the management of hereditary tumor syndromes. 27682646

2016
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: rs1060501224
rs1060501224
CDH1
A 0.700 GeneticVariation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs1060501224
rs1060501224
CDH1
A 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs1060501244
rs1060501244
CDH1
A 0.700 CausalMutation CLINVAR Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1. 26072394

2015
dbSNP: rs1064794231
rs1064794231
CDH1
0.700 GeneticVariation UNIPROT ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes. 25645574

2015
dbSNP: rs1064794231
rs1064794231
CDH1
0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175

2015
dbSNP: rs1064795267
rs1064795267
CDH1
C 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs1131690815
rs1131690815
CDH1
T 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs121964875
rs121964875
CDH1
A 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs121964877
rs121964877
CDH1
T 0.700 CausalMutation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs1555509636
rs1555509636
CDH1
A 0.700 GeneticVariation CLINVAR HBOC multi-gene panel testing: comparison of two sequencing centers. 26022348

2015