Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel. 27798748

2017
dbSNP: rs137853011
rs137853011
CHEK2
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: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR Response to DNA damage of CHEK2 missense mutations in familial breast cancer. 22419737

2012
dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer. 18571837

2008
dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR Trans-activation of the DNA-damage signalling protein kinase Chk2 by T-loop exchange. 16794575

2006
dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population. 15649950

2005
dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 GeneticVariation CLINVAR