F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Hereditary factor II deficiency disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918477
rs121918477
Entrez Id: 2147
Gene Symbol: F2
F2
CUI: C0272317
Disease:
Hereditary factor II deficiency disease 		T 0.700 CausalMutation CLINVAR