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rs61754002(C;C)

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common in clinvar

Is a	genotype
of	rs61754002
Gene	VWF
Chromosome	12
Position	6,072,369
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	4	Von Willebrand disease, type 2N
(A;C)	3	carrier of a Von Willebrand disease allele
(C;C)	0	common in clinvar

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Is a genotype