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rs61749392(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs61749392
GeneVWF
Chromosome12
Position6,019,479
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 3 Von Willebrand disease, type 2B
(C;G) 3.5 von Willebrand disease
(G;G) 0 common in clinvar