RS111033454 SLC26A4

Health Risk Chr 7:107683280 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in SLC26A4
rs121908360 rs1584317722 rs111033308 rs80338848 rs28939086 rs80338849 rs111033244 rs111033303 rs121908361 rs121908364
Ask Dr. Hemsworth about this variant