Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853007
rs137853007
A 0.710 GeneticVariation CLINVAR Response to DNA damage of CHEK2 missense mutations in familial breast cancer. 22419737

2012

dbSNP: rs137853007
rs137853007
A 0.710 GeneticVariation CLINVAR Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2. 12049740

2002

dbSNP: rs137853007
rs137853007
0.710 GeneticVariation BEFREE Here, we describe a CHK2 missense mutation (R145W) in another LFS family. 11719428

2001

dbSNP: rs137853007
rs137853007
A 0.710 GeneticVariation CLINVAR The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis. 11298456

2001

dbSNP: rs137853007
rs137853007
A 0.710 GeneticVariation CLINVAR Here, we describe a CHK2 missense mutation (R145W) in another LFS family. 11719428

2001