rs61748478(G;G)

Von Willebrand disease, type 2N

Is a	genotype
of	rs61748478
Gene	VWF
Chromosome	12
Position	6,044,349
mentioned	by

Magnitude

4

Repute

Bad

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

see discussion at rs61748478