VWF - Gene browser

VWF

von Willebrand factor

HCNC Approved Symbol: VWF (HGNC:12726)
Genomic Coordinates: 12:5,948,877 - 6,124,670 (12p13.31)
Synonyms: F8VWF
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

10Patients

In total, 10 patients were diagnosed with a variant in the VWF gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

010
Patient count

Ecchymoses: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)
Gum bleeding: 3 (30.0%)
Patient Count: 3 (30.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (30.0%)
Epistaxis: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Menorrhagia: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)
Bleeding diathesis: 2 (20.0%)
Patient Count: 2 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (20.0%)