RS111033302 SLC26A4

Health Risk Chr 7:107661643
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
SLC26A4-related disorder
Monogenic hearing loss
Pendred syndrome
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
SLC26A4-related disorder
Monogenic hearing loss
Pendred syndrome
Other Variants in SLC26A4
rs121908360 rs1584317722 rs111033308 rs80338848 rs28939086 rs80338849 rs111033244 rs111033303 rs121908361 rs121908364
Ask Dr. Hemsworth about this variant