RS62643632 VWF
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs62643632, also known as c.2435delC and p.Pro812Argfs, is a SNP in the VWF gene on chromosome 12. T...
Associated Conditions
von Willebrand disease type 3
Hereditary von Willebrand disease
Abnormal bleeding
von Willebrand disease type 1
von Willebrand disease type 2
von Willebrand disorder
von Willebrand disease type 3
Hereditary von Willebrand disease
Abnormal bleeding
von Willebrand disease type 1
von Willebrand disease type 2
von Willebrand disorder
Other Variants in VWF