RS367928692 CDH23
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Usher syndrome type 1D
Pituitary adenoma 5
multiple types
Autosomal recessive nonsyndromic hearing loss 12
Usher syndrome type 1
Hearing loss
autosomal recessive
Retinal dystrophy
CDH23-related disorder
Rare genetic deafness
Usher syndrome type 1D
Pituitary adenoma 5
multiple types
Autosomal recessive nonsyndromic hearing loss 12
Other Variants in CDH23