rs61749392(C;C)

Von Willebrand disease, type 2B

Is a	genotype
of	rs61749392
Gene	VWF
Chromosome	12
Position	6,019,479
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(C;C)	3	Von Willebrand disease, type 2B
(C;G)	3.5	von Willebrand disease
(G;G)	0	common in clinvar

see discussion at rs61749392