RS202033028 SLC26A4

Health Risk Chr 7:107712586
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Associated Conditions
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Inborn genetic diseases
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Inborn genetic diseases
Other Variants in SLC26A4
rs121908360 rs1584317722 rs111033308 rs80338848 rs28939086 rs80338849 rs111033244 rs111033303 rs121908361 rs121908364
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