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rs104894402(C;T)
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Deafness mutation (dominant)
Is a
genotype
of
rs104894402
Gene
GJB2
Chromosome
13
Position
20,189,359
mentioned
by
Magnitude
4
Repute
Bad
Geno
Mag
Summary
(C;C)
0
common in clinvar
(C;T)
4
Deafness mutation (dominant)
see
GJB2
and
deafness
Category
:
Is a genotype
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