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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH23
(D160N)
Single nucleotide variant
(missense variant)
Nonsyndromic genetic hearing loss
GUncertain significance
CDH23
(V2281I +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 12
+3 more
GUncertain significance
CDH23
(N2289S +1 more)
Single nucleotide variant
(missense variant)
Nonsyndromic genetic hearing loss
GUncertain significance
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