RS80338848 SLC26A4
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What This Variant Does
"rs80338848, also known as L236P, 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
Hearing impairment
SLC26A4-related disorder
Inborn genetic diseases
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
Hearing impairment
SLC26A4-related disorder
Inborn genetic diseases
Other Variants in SLC26A4