Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912628
rs121912628
RAD50
T 0.700 GeneticVariation CLINVAR The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies. 28376765

2017
dbSNP: rs1060501941
rs1060501941
RAD50
T 0.700 GeneticVariation CLINVAR Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care. 26786923

2016
dbSNP: rs1247689593
rs1247689593
RAD50
T 0.700 GeneticVariation CLINVAR Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. 26822949

2016
dbSNP: rs587782895
rs587782895
RAD50
C 0.700 CausalMutation CLINVAR Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. 26824983

2016
dbSNP: rs121912628
rs121912628
RAD50
T 0.700 GeneticVariation CLINVAR Patterns and functional implications of rare germline variants across 12 cancer types. 26689913

2015
dbSNP: rs149201802
rs149201802
RAD50
G 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: rs760146707
rs760146707
RAD50
G 0.700 GeneticVariation 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: rs121912628
rs121912628
RAD50
T 0.700 GeneticVariation CLINVAR Functional characterization connects individual patient mutations in ataxia telangiectasia mutated (ATM) with dysfunction of specific DNA double-strand break-repair signaling pathways. 21778326

2011
dbSNP: rs121912628
rs121912628
RAD50
T 0.700 GeneticVariation CLINVAR Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. 19409520

2009
dbSNP: rs149201802
rs149201802
RAD50
G 0.700 CausalMutation CLINVAR Mutational analysis of thirty-two double-strand DNA break repair genes in breast and pancreatic cancers. 18281469

2008
dbSNP: rs760146707
rs760146707
RAD50
G 0.700 GeneticVariation CLINVAR RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. 16474176

2006
dbSNP: rs760146707
rs760146707
RAD50
G 0.700 GeneticVariation CLINVAR Evaluation of RAD50 in familial breast cancer predisposition. 16385572

2006
dbSNP: rs760146707
rs760146707
RAD50
G 0.700 GeneticVariation CLINVAR Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility. 14684699

2003
dbSNP: rs121912628
rs121912628
RAD50
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912629
rs121912629
RAD50 ; TH2LCRR
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554096791
rs1554096791
RAD50
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554098250
rs1554098250
RAD50
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1561635887
rs1561635887
RAD50
CTA 0.700 GeneticVariation CLINVAR

dbSNP: rs397507178
rs397507178
RAD50
TA 0.700 CausalMutation CLINVAR

dbSNP: rs587782090
rs587782090
RAD50
T 0.700 CausalMutation CLINVAR

dbSNP: rs772468452
rs772468452
RAD50
T 0.700 CausalMutation CLINVAR

dbSNP: rs876659005
rs876659005
RAD50
TA 0.700 GeneticVariation CLINVAR

dbSNP: rs878854799
rs878854799
RAD50 ; TH2LCRR
T 0.700 GeneticVariation CLINVAR