rs104894413(A;G)

Carrier of a recessive deafness mutation

Is a	genotype
of	rs104894413
Gene	GJB2
Chromosome	13
Position	20,189,451
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