Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554098706
rs1554098706
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CT 0.700 CausalMutation CLINVAR Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. 26824983 2016
dbSNP: rs1554098706
rs1554098706
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CT 0.700 CausalMutation CLINVAR Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. 25452441 2015
dbSNP: rs1554098706
rs1554098706
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CT 0.700 CausalMutation CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289 2014