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rs104894402(C;T)

From SNPedia
Deafness mutation (dominant)
Is agenotype
ofrs104894402
GeneGJB2
Chromosome13
Position20,189,359
mentionedby
Magnitude4
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 4 Deafness mutation (dominant)

see GJB2 and deafness