SERPINE1, serpin family E member 1, 5054

N. diseases: 770; N. variants: 23
Disease: Hereditary protein S deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2584611
Disease: Hereditary protein S deficiency
Hereditary protein S deficiency 		0.010 GeneticVariation disease BEFREE In the present study, the 4G-5G dimorphism was determined in 349 individuals from 21 thrombophilic families with hereditary protein S deficiency and in 140 unrelated healthy controls. 9569196 1998