rs61749380(C;C)

common in clinvar

Is a	genotype
of	rs61749380
Gene	VWF
Chromosome	12
Position	6,019,564
mentioned	by

Magnitude

0

Repute

Good

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