F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Reduced prothrombin activity ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776618390
rs776618390
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C4021097
Disease:
Reduced prothrombin activity 		C 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019