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rs61749387(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs61749387
GeneVWF
Chromosome12
Position6,019,496
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Von Willebrand disease, type 2B
(T;T) 3 Von Willebrand disease, type 2B