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rs104894407(A;G)
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Carrier of a recessive deafness mutation
Is a
genotype
of
rs104894407
Gene
GJB2
Chromosome
13
Position
20,189,450
mentioned
by
Magnitude
3
Repute
Bad
Geno
Mag
Summary
(A;G)
3
Carrier of a recessive deafness mutation
(C;G)
4
Deafness mutation (dominant)
(G;G)
0
common in clinvar
see
GJB2
and
deafness
Category
:
Is a genotype
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