rs61748511(C;C)

Von Willebrand disease, type 1

Is a	genotype
of	rs61748511
Gene	VWF
Chromosome	12
Position	6,022,833
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(C;C)	3	Von Willebrand disease, type 1
(C;T)	3.5	von Willebrand disease
(T;T)	0	common in clinvar

see discussion at rs61748511