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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH23, CDH23-AS1
(D94H)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 12
GUncertain significance
CDH23
(L369P)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 12
GUncertain significance