RS111033312 SLC26A4

Health Risk Chr 7:107698111 snv splice donor variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 4
Pendred syndrome
Rare genetic deafness
Pendred syndrome
Autosomal recessive nonsyndromic hearing loss 4
Autosomal recessive nonsyndromic hearing loss 4
Population Frequencies
gnomAD ALL
100%
Other Variants in SLC26A4
rs121908360 rs1584317722 rs111033308 rs80338848 rs28939086 rs80338849 rs111033244 rs111033303 rs121908361 rs121908364
Ask Dr. Hemsworth about this variant