rs61749380(T;T)

Von Willebrand disease, type 2M

Is a	genotype
of	rs61749380
Gene	VWF
Chromosome	12
Position	6,019,564
mentioned	by

Magnitude

3

Repute

Bad

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

see discussion at rs61749380