EPHB2, EPH receptor B2, 2048

N. diseases: 649; N. variants: 19
Disease: Prostate cancer, familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931456
Disease: Prostate cancer, familial
Prostate cancer, familial 		0.310 GeneticVariation disease BEFREE We have previously shown an association between an EphB2 germline nonsense variant and risk of familial prostate cancer among African American Men (AAM). 21603658 2011
CUI: C2931456
Disease: Prostate cancer, familial
Prostate cancer, familial 		0.310 SusceptibilityMutation disease ORPHANET A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history. 16155194 2006