RS28939086 SLC26A4
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What This Variant Does
"rs28939086, also known as T416P, is a SNP in the SLC26A4 gene associated with the hearing loss condi...
Associated Conditions
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Inborn genetic diseases
Monogenic hearing loss
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Inborn genetic diseases
Monogenic hearing loss
Other Variants in SLC26A4