rs61749392(G;G)

common in clinvar

Is a	genotype
of	rs61749392
Gene	VWF
Chromosome	12
Position	6,019,479
mentioned	by

Magnitude

0

Repute

Good

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