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rs104894398(G;T)
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Carrier of a recessive deafness mutation
Is a
genotype
of
rs104894398
Gene
GJB2
Chromosome
13
Position
20,189,443
mentioned
by
Magnitude
3
Repute
Bad
Geno
Mag
Summary
(G;G)
0
common in clinvar
(G;T)
3
Carrier of a recessive deafness mutation
see
GJB2
and
deafness
Category
:
Is a genotype
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