RS397516411 SLC26A4-AS1;SLC26A4
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Nonpapillary renal cell carcinoma
Inborn genetic diseases
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
SLC26A4-related disorder
Nonpapillary renal cell carcinoma
Inborn genetic diseases