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: rs1060501949
rs1060501949
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. 19409520 2009
dbSNP: rs1060501949
rs1060501949
Entrez Id: 10111
Gene Symbol: RAD50
RAD50
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR Evaluation of RAD50 in familial breast cancer predisposition. 16385572 2006