rs62643630(T;T)

Von Willebrand disease, type 2N

Is a	genotype
of	rs62643630
Gene	VWF
Chromosome	12
Position	6,044,322
mentioned	by

Magnitude

4

Repute

Bad

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

see discussion at rs62643630