RS111033244 SLC26A4
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What This Variant Does
"rs111033244, also known as E384G, 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
SLC26A4-related disorder
Pendred syndrome
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
SLC26A4-related disorder
Other Variants in SLC26A4