Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917885
rs121917885
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Identification of a new dysfunctional platelet P2Y12 receptor variant associated with bleeding diathesis. 25428217

2015
dbSNP: rs121917886
rs121917886
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Identification of a new dysfunctional platelet P2Y12 receptor variant associated with bleeding diathesis. 25428217

2015
dbSNP: rs121917885
rs121917885
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding. 12578987

2003
dbSNP: rs121917886
rs121917886
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding. 12578987

2003
dbSNP: rs121917885
rs121917885
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Identification of the platelet ADP receptor targeted by antithrombotic drugs. 11196645

2001
dbSNP: rs121917886
rs121917886
P2RY12 ; MED12L
0.800 GeneticVariation UNIPROT Identification of the platelet ADP receptor targeted by antithrombotic drugs. 11196645

2001
dbSNP: rs121917885
rs121917885
P2RY12 ; MED12L
T 0.800 CausalMutation CLINVAR

dbSNP: rs121917886
rs121917886
P2RY12 ; MED12L
A 0.800 CausalMutation CLINVAR

dbSNP: rs1560045738
rs1560045738
P2RY12 ; MED12L
A 0.700 CausalMutation CLINVAR

dbSNP: rs755459581
rs755459581
P2RY12 ; MED12L
G 0.700 CausalMutation CLINVAR