RS397517334 CDH23

Health Risk Chr 10:71777900
Upload your DNA to see your genotype for this variant.
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
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908351 rs121908352
Ask Dr. Hemsworth about this variant