KEGG   VARIANT: 2155v1
Entry
2155v1                      Variant                                
Name
F7 mutation
Type
Loss of function
Gene
F7  coagulation factor VII [KO:K01320]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 613878
Network
nt06514  Coagulation cascade
Disease
H01730  Myocardial infarction
H02256  Factor VII deficiency
Reference
PMID:28350321
  Authors
Napolitano M, Siragusa S, Mariani G
  Title
Factor VII Deficiency: Clinical Phenotype, Genotype and Therapy.
  Journal
J Clin Med 6:E38 (2017)
DOI:10.3390/jcm6040038
Reference
PMID:10984565
  Authors
Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R
  Title
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.
  Journal
N Engl J Med 343:774-80 (2000)
DOI:10.1056/NEJM200009143431104
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