RS111033205 SLC26A4
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What This Variant Does
"Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genoty...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
Pendred syndrome
Wolff-Parkinson-White pattern
SLC26A4-related disorder
Ear malformation
Monogenic hearing loss
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
Pendred syndrome
Wolff-Parkinson-White pattern
SLC26A4-related disorder
Ear malformation
Other Variants in SLC26A4