rs61750612(C;C)

common in clinvar

Is a	genotype
of	rs61750612
Gene	VWF
Chromosome	12
Position	6,013,544
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Von Willebrand disease; carrier or Type 1
(T;T)	4	Von Willebrand disease, type 3