VWF

von Willebrand factor
OMIM: 613160, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels
Green VWF in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.52

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
Phenotypes
  • von Willebrand disease, type 1, MIM#193400
  • von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM#613554
  • von Willibrand disease, type 3, MIM#277480
Green VWF in Mendeliome


Version 1.2302

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • von Willebrand disease, type 1, MIM# 193400
  • von Willebrand disease, type 3 , MIM#277480
  • von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM# 613554
Green VWF in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3)
Amber VWF in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • BabySeq Category B gene
Phenotypes
  • von Willebrand disease
Amber VWF in Prepair 1000+


Level 2: Screening
Version 1.1566

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Mackenzie's Mission
Phenotypes
  • von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3)
Amber VWF in BabyScreen+ newborn screening


Level 2: Screening
Version 1.116

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category B gene
  • Expert Review Amber
Phenotypes
  • von Willebrand disease
Green VWF in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • von Willebrand disease, type 1, MIM#193400
  • von Willibrand disease, type 3, MIM#277480
  • von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM#613554