Annotation Detail
Information
- Associated Genes
- FGG
- Associated Variants
-
FGG c.*216C>T
FGG c.*216C>T - Associated Disease
- myocardial infarction
- Source Database
- DisGeNET
- Description
- A functional single nucleotide polymorphism (SNP) in the 3' untranslated region of the FGG gene (FGG 10034C>T, rs2066865) has been associated with deep venous thrombosis and myocardial infarction.
- Pubmed
- 20709368
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.0153738357517182
- Year of publication
- 2010
Drugs