F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Hypoprothrombinemias ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757240974
rs757240974
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C4722227
Disease:
Hypoprothrombinemias 		0.010 GeneticVariation BEFREE Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg382-Cys), Dhahran (Arg271-His), and hypoprothrombinemia. 8839854 1996