RS111033303 SLC26A4

Health Risk Chr 7:107674970
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Rare genetic deafness
Hearing impairment
SLC26A4-related disorder
Ear malformation
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Rare genetic deafness
Hearing impairment
SLC26A4-related disorder
Ear malformation
Other Variants in SLC26A4
rs121908360 rs1584317722 rs111033308 rs80338848 rs28939086 rs80338849 rs111033244 rs121908361 rs121908364 rs121908362
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