RS139287714 CDH23

Health Risk Chr 10:71646468 snv missense variant
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Associated Conditions
Usher syndrome type 1
Inborn genetic diseases
Usher syndrome type 1
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.6%
1kG ALL
0.1%
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