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rs61750595(C;T)

From SNPedia

likely miscall in Ancestry V2.0 datasets; otherwise, carrier of a Von Willebrand disease allele
Is agenotype
ofrs61750595
GeneVWF
Chromosome12
Position6,018,443
mentionedby
Magnitude3
ReputeBad
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