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rs104894398(G;T)

From SNPedia
Carrier of a recessive deafness mutation
Is agenotype
ofrs104894398
GeneGJB2
Chromosome13
Position20,189,443
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a recessive deafness mutation

see GJB2 and deafness