F5, coagulation factor V, 2153

N. diseases: 369; N. variants: 52
Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6025
rs6025
Entrez Id: 2153
Gene Symbol: F5
F5
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE Factor V Leiden, an R506Q mutation in the gene coding for factor V, is the most common cause of familial thrombosis and could be a potentiating factor. 8592550 1996