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rs104894413(A;G)

From SNPedia

Carrier of a recessive deafness mutation
Is agenotype
ofrs104894413
GeneGJB2
Chromosome13
Position20,189,451
mentionedby
Magnitude3
ReputeBad
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