rs1188383936, F2

N. diseases: 102
Disease: Atherothrombosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
0.010 GeneticVariation BEFREE We report a case of myocardial infarction at a young age in a subject heterozygous for the G20210A prothrombin gene variant and homozygous for the C677T MTHFR polymorphism, who presented a strong family history of atherothrombosis. 17920139 2008