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rs61748478(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs61748478
GeneVWF
Chromosome12
Position6,044,349
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 carrier of a Von Willebrand disease allele
(G;G) 4 Von Willebrand disease, type 2N