Familial hypercholesterolaemia

Gene: F7

Red List (low evidence)

F7 (coagulation factor VII)
EnsemblGeneIds (GRCh38): ENSG00000057593
EnsemblGeneIds (GRCh37): ENSG00000057593
OMIM: 613878, Gene2Phenotype
F7 is in 4 panels

1 review

Ellen Thomas (Genomics England)

Red List (low evidence)

Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Factor VII deficiency, 227500
  • {Myocardial infarction, decreased susceptibility to}, 608446
OMIM
613878
Clinvar variants
Variants in F7
Penetrance
Complete
Panels with this gene

History Filter Activity

7 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

F7 was added to Familial hypercholesterolaemiapanel. Sources: Radboud University Medical Center, Nijmegen