rs61749387(C;T)

Von Willebrand disease, type 2B

Is a	genotype
of	rs61749387
Gene	VWF
Chromosome	12
Position	6,019,496
mentioned	by

Magnitude

3

Repute

Bad

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

see discussion at rs61749387