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i5049104

From SNPedia

23andMe dataI5049104
23andMe searchI5049104
opensnpI5049104
Gene (via rs)VWF

aliasrs61750595
Rs_StabilizedOrientationminus
RsGeno 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

rs61750595

Von Willebrand disease