rs111033220(T;T)

Pendred syndrome (hearing loss)

Is a	genotype
of	rs111033220
Gene	SLC26A4
Chromosome	7
Position	107,690,203
mentioned	by

Magnitude

5

Repute

Bad

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a mutation for Pendred syndrome (hearing loss)
(T;T)	5	Pendred syndrome (hearing loss)

see rs111033220