RS121908351 CDH23

Health Risk Chr 10:71732292
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 12
Usher syndrome type 1
Pituitary adenoma 5
multiple types
Usher syndrome
Usher syndrome type 1D
Autosomal recessive nonsyndromic hearing loss 12
Usher syndrome type 1
Pituitary adenoma 5
multiple types
Usher syndrome
Usher syndrome type 1D
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908352 rs796051861
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