SERPINE1, serpin family E member 1, 5054

N. diseases: 770; N. variants: 23
Disease: Factor V Leiden mutation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799889
rs1799889
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1
CUI: C0584960
Disease:
Factor V Leiden mutation 		0.010 GeneticVariation BEFREE Our findings supported that PAI-1 rs1799889 polymorphism may serve as one of the predisposing factors of VTE in both Caucasians and East Asians, especially in these with DVT and these with Factor V Leiden mutation. 31701558 2019