rs111033212(C;C)

Pendred Syndrome (deafness)

Is a	genotype
of	rs111033212
Gene	SLC26A4
Chromosome	7
Position	107,689,054
mentioned	by

Magnitude

5

Repute

Bad

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