RS727504455 CDH23

Health Risk Chr 10:71646537
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Retinal dystrophy
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Retinal dystrophy
Autosomal recessive nonsyndromic hearing loss 12
Other Variants in CDH23
rs121908347 rs111033270 rs796051860 rs727502931 rs121908348 rs121908349 rs121908350 rs111033271 rs121908351 rs121908352
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