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rs137852260(T;T)
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common in clinvar
Is a
genotype
of
rs137852260
Gene
F9
Chromosome
X
Position
139,561,829
mentioned
by
Magnitude
0
Repute
Good
Geno
Mag
Summary
(C;C)
5.5
Hemophilia B (severity varies)
(C;T)
3.5
Carrier of a Hemophilia B mutation
(T;T)
0
common in clinvar
Category
:
Is a genotype
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