Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing. 30264118

2018

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR A Life Potentially Saved Through Hereditary Cancer Panel Testing. 28195815

2017

dbSNP: rs876660771
rs876660771
A 0.700 CausalMutation CLINVAR Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond. 26182300

2015

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Hereditary diffuse gastric cancer: translation of CDH1 germline mutations into clinical practice. 20373070

2010

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR A short guide to hereditary diffuse gastric cancer. 19725995

2007

dbSNP: rs876660771
rs876660771
A 0.700 CausalMutation CLINVAR A short guide to hereditary diffuse gastric cancer. 19725995

2007

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Familial gastric cancer - aetiology and pathogenesis. 16997156

2006

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Genetic screening for familial gastric cancer. 20233471

2004

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Genetic screening for hereditary diffuse gastric cancer. 12647996

2003

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR Hereditary diffuse gastric cancer. 11665720

2001

dbSNP: rs876660771
rs876660771
A 0.700 CausalMutation CLINVAR Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer. 10973239

2000

dbSNP: rs876660771
rs876660771
A 0.700 CausalMutation CLINVAR E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer. 10477433

1999

dbSNP: rs876660771
rs876660771
A 0.700 GeneticVariation CLINVAR E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer. 10477433

1999