RS111033308 SLC26A4

Health Risk Chr 7:107695984
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What This Variant Does
"A mutation in PDS causes non-syndromic recessive deafness. Functional differences of the PDS gene pr...
Associated Conditions
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Hearing impairment
Deafness
Pendred syndrome
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Hearing impairment
Deafness
Pendred syndrome
Other Variants in SLC26A4
rs121908360 rs1584317722 rs80338848 rs28939086 rs80338849 rs111033244 rs111033303 rs121908361 rs121908364 rs121908362
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