Annotation Detail
Information
- Associated Genes
- F2
- Associated Variants
-
F2 c.*97G>A
(
ENST00000311907.10 )
F2 c.*97G>A ( ENST00000311907.10 ) - Associated Disease
- Myoclonic Epilepsy, Juvenile
- Source Database
- DisGeNET
- Description
- Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy.
- Pubmed
- 25992517
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2014
Drugs