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Details of Gene

Item Details
Gene/Locus name

F5 (also called )

Long Name

coagulation factor V (OMIM 612309)

Associated Disorders

OMIM 614389 : Pregnancy loss, recurrent, susceptibility to, 1
OMIM 188055 : Thrombophilia due to activated protein C resistance
OMIM 601367 : Stroke, ischemic, susceptibility to
OMIM 188055 : Thrombophilia, susceptibility to, due to factor V Leiden
OMIM 227400 : Factor V deficiency
OMIM 600880 : Budd-Chiari syndrome

Interpretation / Comment

Laboratory methods do not necessarily identify all of the clinically significant variants in a gene. The failure to identify a variant does not necessarily mean that the gene is normal. Variants in a gene may cause more than one disease, and the identification of a clinically significant variant does not necessarily indicate the specific disease that the patient or relatives may be at risk of developing. Conversely, the disease/s associated with a gene might also be caused by mutations in other genes, and the failure to identify a clinically significant variant in one gene does not necessarily alter the clinical diagnosis or risk for relatives.

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