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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH23
(G1025D)
Single nucleotide variant
(missense variant)
CDH23-related disorder
+5 more
GConflicting classifications of pathogenicity
CDH23
(R2608H +1 more)
Single nucleotide variant
(missense variant)
CDH23-related disorder
+7 more
GConflicting classifications of pathogenicity