RS370983472 CDH23

Health Risk Chr 10:71799629
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Usher syndrome type 1
Usher syndrome type 1D
Usher syndrome
Pituitary adenoma 5
multiple types
Retinal dystrophy
Rare genetic deafness
Usher syndrome type 1
Usher syndrome type 1D
Usher syndrome
Pituitary adenoma 5
multiple types
Retinal dystrophy
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908351 rs121908352
Ask Dr. Hemsworth about this variant