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rs61748497(C;T)

From SNPedia

carrier of a Von Willebrand disease allele
Is agenotype
ofrs61748497
GeneVWF
Chromosome12
Position6,025,624
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 4 Von Willebrand disease, type 2N
(C;T) 3 carrier of a Von Willebrand disease allele
(T;T) 0 common in clinvar

see discussion at rs61748497