rs61749397(G;G)

common in clinvar

Is a	genotype
of	rs61749397
Gene	VWF
Chromosome	12
Position	6,019,472
mentioned	by

Magnitude

0

Repute

Good

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