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rs104894406(G;T)

From SNPedia
Deafness mutation (dominant)
Is agenotype
ofrs104894406
GeneGJB2
Chromosome13
Position20,188,977
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 4 Deafness mutation (dominant)

see GJB2 and deafness