RS121908350 CDH23

Health Risk Chr 10:71732151
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What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 1D
Hearing loss
autosomal recessive
Usher syndrome type 1D
Hearing loss
autosomal recessive
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs111033271 rs121908351 rs121908352 rs796051861
Ask Dr. Hemsworth about this variant