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rs104894407(C;G)

From SNPedia

Deafness mutation (dominant)
Is agenotype
ofrs104894407
GeneGJB2
Chromosome13
Position20,189,450
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(A;G) 3 Carrier of a recessive deafness mutation
(G;G) 0 common in clinvar

see GJB2 and deafness