rs61748477(T;T)

Von Willebrand disease, type 2N

Is a	genotype
of	rs61748477
Gene	VWF
Chromosome	12
Position	6,044,361
mentioned	by

Magnitude

4

Repute

Bad

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

see discussion at rs61748477