rs61748497(C;C)

Von Willebrand disease, type 2N

Is a	genotype
of	rs61748497
Gene	VWF
Chromosome	12
Position	6,025,624
mentioned	by

Magnitude

4

Repute

Bad

Geno	Mag	Summary
(C;C)	4	Von Willebrand disease, type 2N
(C;T)	3	carrier of a Von Willebrand disease allele
(T;T)	0	common in clinvar

see discussion at rs61748497