RS111033305 SLC26A4
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Hearing loss
autosomal recessive
Ear malformation
Rare genetic deafness
Hearing loss
autosomal recessive
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Other Variants in SLC26A4