Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.710 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | GeneticVariation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.810 | SusceptibilityMutation | CLINVAR | Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia. | 11443298 | 2001 |
|||
|
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 |
|||
|
0.800 | GeneticVariation | GWASDB | A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. | 17434096 | 2007 |
||||
|
0.800 | GeneticVariation | GWASCAT | A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. | 17434096 | 2007 |
||||
|
0.720 | GeneticVariation | GWASDB | A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. | 17206144 | 2007 |
||||
|
T | 0.820 | GeneticVariation | GWASCAT | Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. | 18991354 | 2008 |
|||
|
T | 0.820 | GeneticVariation | GWASDB | Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. | 18991354 | 2008 |
|||
|
A | 0.890 | GeneticVariation | GWASDB | Genomewide association studies of stroke. | 19369658 | 2009 |
|||
|
A | 0.890 | GeneticVariation | GWASCAT | Genomewide association studies of stroke. | 19369658 | 2009 |
|||
|
A | 0.810 | SusceptibilityMutation | CLINVAR | The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. | 19652888 | 2009 |
|||
|
0.700 | GeneticVariation | GWASDB | Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. | 21957438 | 2011 |
||||
|
0.700 | GeneticVariation | GWASDB | Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. | 21957438 | 2011 |