F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Acute myocardial infarction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0155626
Disease:
Acute myocardial infarction 		0.020 GeneticVariation BEFREE Analysis of polymorphisms Leiden Factor V G1691A and prothrombin G20210A as risk factors for acute myocardial infarction. 21918818 2011
dbSNP: rs899127658
rs899127658
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0155626
Disease:
Acute myocardial infarction 		0.020 GeneticVariation BEFREE In a large cohort of young AMI patients the gain-of-function variant F5 G1691A was associated with an increased risk of AMI. 20626623 2010