RS202052174 CDH23

Health Risk Chr 10:71803371
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What This Variant Does
"CLNSIG=4
Associated Conditions
Retinitis pigmentosa-deafness syndrome
Neurodevelopmental abnormality
Usher syndrome type 1D
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Pituitary adenoma 5
multiple types
Retinal dystrophy
Retinitis pigmentosa-deafness syndrome
Neurodevelopmental abnormality
Usher syndrome type 1D
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Pituitary adenoma 5
multiple types
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908351 rs121908352
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