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rs111033212(C;C)

From SNPedia
Pendred Syndrome (deafness)
Is agenotype
ofrs111033212
GeneSLC26A4
Chromosome7
Position107,689,054
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(C;C) 5 Pendred Syndrome (deafness)
(C;T) 3 Carrier of a Pendred syndrome (deafness) mutation
(T;T) 0 common in clinvar

See rs111033212