ClinGen Knowledge Base | Clinical Genome Resource

F5

Name: F5
HGNC ID: HGNC:3542
Cytogenetic Location: 1q24.2
Haploinsufficiency: Associated with Autosomal Recessive Phenotype
Triplosensitivity: No Evidence

External Resources: View external resources
ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

F5 - congenital factor V deficiency | MONDO:0009210

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype	01/11/2018	View report
Clinical Actionability	View report for scoring details	04/02/2018	View report

F5 - thrombophilia due to activated protein C resistance | MONDO:0008560

Curated by	Classification	Date	Report
Clinical Actionability	View report for scoring details	04/09/2018	View report

F5

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype	01/11/2018	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	01/11/2018	View report

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.