Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1333600
Disease: Hereditary Malignant Neoplasm
Hereditary Malignant Neoplasm
0.010 GeneticVariation disease BEFREE The clinical utility of BRIP1 mutations in a familial cancer context is compromised by the conflicting interpretation of "variants of uncertain significance" (VUS). 30230034 2019