rs61750595(T;T)

likely miscall in Ancestry V2.0 datasets; otherwise, Von Willebrand disease, type 3

Is a	genotype
of	rs61750595
Gene	VWF
Chromosome	12
Position	6,018,443
mentioned	by

Magnitude

4

Repute

Bad

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	likely miscall in Ancestry V2.0 datasets; otherwise, carrier of a Von Willebrand disease allele
(T;T)	4	likely miscall in Ancestry V2.0 datasets; otherwise, Von Willebrand disease, type 3

see discussion at rs61750595