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rs41276738(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs41276738
GeneVWF
Chromosome12
Position6,034,812
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of a Von Willebrand disease allele
(T;T) 4 Von Willebrand disease, type 1