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rs61749387(C;C)
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common in clinvar
Is a
genotype
of
rs61749387
Gene
VWF
Chromosome
12
Position
6,019,496
mentioned
by
Magnitude
0
Repute
Good
Geno
Mag
Summary
(C;C)
0
common in clinvar
(C;T)
3
Von Willebrand disease, type 2B
(T;T)
3
Von Willebrand disease, type 2B
Category
:
Is a genotype
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