rs104894401(A;G)

Deafness mutation (dominant)

Is a	genotype
of	rs104894401
Gene	GJB2
Chromosome	13
Position	20,189,154
mentioned	by

Magnitude

4

Repute

Bad

Geno	Mag	Summary
(A;G)	4	Deafness mutation (dominant)
(G;G)	0	common in clinvar

see GJB2 and deafness