VWF

von Willebrand factor
OMIM: 613160, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green VWF in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	2 reviews	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	1 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	0 reviews	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	0 reviews	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	1 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	0 reviews	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	0 reviews	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