Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72653706
rs72653706
ABCC6
A 0.710 CausalMutation CLINVAR

dbSNP: rs121908029
rs121908029
LDLR
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
PIK3CA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554810066
rs1554810066
ENG ; LOC105379841
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555517253
rs1555517253
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs1568362252
rs1568362252
NOTCH3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs199474657
rs199474657
ND1 ; ND2 ; TRNL1
G 0.700 CausalMutation CLINVAR

dbSNP: rs28933696
rs28933696
NOTCH3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs63749796
rs63749796
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs63751241
rs63751241
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs72664204
rs72664204
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs72664207
rs72664207
ABCC6
C 0.700 CausalMutation CLINVAR

dbSNP: rs754360599
rs754360599
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia. 11443298

2001
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR The prothrombin 3'end formation signal reveals a unique architecture that is sensitive to thrombophilic gain-of-function mutations. 15059842

2004
dbSNP: rs2230500
rs2230500
PRKCH
0.720 GeneticVariation GWASDB A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. 17206144

2007
dbSNP: rs7506045
rs7506045
IMPA2
0.800 GeneticVariation GWASDB A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. 17434096

2007
dbSNP: rs7506045
rs7506045
IMPA2
0.800 GeneticVariation GWASCAT A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. 17434096

2007
dbSNP: rs2200733
rs2200733 		T 0.820 GeneticVariation GWASCAT Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. 18991354

2008
dbSNP: rs2200733
rs2200733 		T 0.820 GeneticVariation GWASDB Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. 18991354

2008
dbSNP: rs12425791
rs12425791 		A 0.890 GeneticVariation GWASDB Genomewide association studies of stroke. 19369658

2009
dbSNP: rs12425791
rs12425791 		A 0.890 GeneticVariation GWASCAT Genomewide association studies of stroke. 19369658

2009
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. 19652888

2009
dbSNP: rs11044400
rs11044400 		0.700 GeneticVariation GWASDB Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. 21957438

2011
dbSNP: rs11240065
rs11240065
LINC00624
0.700 GeneticVariation GWASDB Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. 21957438

2011