Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR Comparative genomic analysis of primary tumors and metastases in breast cancer. 27028851

2016

dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR Prevalence of the CHEK2 R95* germline mutation. 27708748

2016

dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015

dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory. 24506336

2014

dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study. 21244692

2011

dbSNP: rs587781269
rs587781269
A 0.700 CausalMutation CLINVAR CHEK2 mutations affecting kinase activity together with mutations in TP53 indicate a functional pathway associated with resistance to epirubicin in primary breast cancer. 18725978

2008