Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. 29577179

2019
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing. 28873162

2017
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: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients. 23264079

2013
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Searching for E-cadherin gene mutations in early onset diffuse gastric cancer and hereditary diffuse gastric cancer in Korean patients. 23264079

2013
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR To accomplish our objective we characterized the effect of eleven HDGC CDH1 germline missense mutations (T118R, L214P, G239R, A298T, T340A, P373L, R749W, E757K, E781D, P799R and V832M) on cell motility. 19268661

2009
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR To accomplish our objective we characterized the effect of eleven HDGC CDH1 germline missense mutations (T118R, L214P, G239R, A298T, T340A, P373L, R749W, E757K, E781D, P799R and V832M) on cell motility. 19268661

2009
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. 17545690

2007
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. 17545690

2007
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR Identification of seven novel germline mutations in the human E-cadherin (CDH1) gene. 17221870

2007
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR Identification of seven novel germline mutations in the human E-cadherin (CDH1) gene. 17221870

2007
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR A short guide to hereditary diffuse gastric cancer. 19725995

2007
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 GeneticVariation CLINVAR A model to infer the pathogenic significance of CDH1 germline missense variants. 16924464

2006
dbSNP: rs587780537
rs587780537
CDH1
A 0.700 CausalMutation CLINVAR A model to infer the pathogenic significance of CDH1 germline missense variants. 16924464

2006