Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786202259
rs786202259
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study. 24894818 2014
dbSNP: rs786202259
rs786202259
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR Mre11-Rad50-Nbs1 conformations and the control of sensing, signaling, and effector responses at DNA double-strand breaks. 21035407 2010
dbSNP: rs786202259
rs786202259
Entrez Id: 10111;101927761
Gene Symbol: RAD50;TH2LCRR
RAD50;TH2LCRR
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 GeneticVariation CLINVAR