RS187447337 SLC26A4
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Hearing impairment
Inborn genetic diseases
SLC26A4-related disorder
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Hearing impairment
Inborn genetic diseases
SLC26A4-related disorder
Other Variants in SLC26A4