RS114745089 CDH23

Health Risk Chr 10:71779375 snv missense variant
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Associated Conditions
Autosomal recessive nonsyndromic hearing loss 12
Usher syndrome type 1D
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 12
Usher syndrome type 1D
Usher syndrome type 1
Population Frequencies
gnomAD ALL
100%
1kG AFR
98.8%
1kG ALL
99.7%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908351 rs121908352
Ask Dr. Hemsworth about this variant