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rs1800386(A;A)

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common in complete genomics

Is a	genotype
of	rs1800386
Gene	VWF
Chromosome	12
Position	6,018,667
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	0	common in complete genomics
(A;G)	3	association with Von Willebrand disease type 1
(G;G)	3	association with Von Willebrand disease type 1

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Is a genotype