RS111033307 SLC26A4
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What This Variant Does
"rs111033307, also known as L445W, is a SNP in the SLC26A4 gene associated with the hearing loss cond...
Associated Conditions
Pendred syndrome
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Monogenic hearing loss
Pendred syndrome
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Monogenic hearing loss
Other Variants in SLC26A4