Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Bleeding Disorder Due To P2RY12 Defect
CUI: C1853278
Disease: Bleeding Disorder Due To P2RY12 Defect
0.800 GeneticVariation UNIPROT Identification of a new dysfunctional platelet P2Y12 receptor variant associated with bleeding diathesis. 25428217 2015
Bleeding Disorder Due To P2RY12 Defect
CUI: C1853278
Disease: Bleeding Disorder Due To P2RY12 Defect
0.800 GeneticVariation UNIPROT Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding. 12578987 2003
Bleeding Disorder Due To P2RY12 Defect
CUI: C1853278
Disease: Bleeding Disorder Due To P2RY12 Defect
0.800 GeneticVariation UNIPROT Identification of the platelet ADP receptor targeted by antithrombotic drugs. 11196645 2001
Bleeding Disorder Due To P2RY12 Defect
CUI: C1853278
Disease: Bleeding Disorder Due To P2RY12 Defect
0.800 CausalMutation CLINVAR