RS121908362 SLC26A4
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121908362, also known as H723R, is a SNP in the SLC26A4 gene associated with the hearing loss cond...
Associated Conditions
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Congenital portosystemic shunt
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Congenital portosystemic shunt
Other Variants in SLC26A4