rs61748511(T;T)

common in clinvar

Is a	genotype
of	rs61748511
Gene	VWF
Chromosome	12
Position	6,022,833
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	3	Von Willebrand disease, type 1
(C;T)	3.5	von Willebrand disease
(T;T)	0	common in clinvar