rs61750579(T;T)

common in clinvar

Is a	genotype
of	rs61750579
Gene	VWF
Chromosome	12
Position	6,018,598
mentioned	by

Magnitude

0

Repute

Good

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