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rs61749392(G;G)

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common in clinvar

Is a	genotype
of	rs61749392
Gene	VWF
Chromosome	12
Position	6,019,479
mentioned	by

0

Good

Geno	Mag	Summary
(C;C)	3	Von Willebrand disease, type 2B
(C;G)	3.5	von Willebrand disease
(G;G)	0	common in clinvar

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Is a genotype