Annotation Detail
Information
- Associated Genes
- SUPT7L
- Associated Variants
-
FGG c.*216C>T
FGG c.*216C>T - Associated Disease
- Deep Vein Thrombosis
- Source Database
- DisGeNET
- Description
- Recently, a haplotype-tagging single nucleotide polymorphism characterized by a C to T substitution at nucleotide 10034 of the fibrinogen gamma gene (FGG 10034C>T, rs2066865), has been proposed as a novel risk factor for deep venous thrombosis (DVT).
- Pubmed
- 17445871
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000542883744160607
- Year of publication
- 2007
Drugs