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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDH23
(R191Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
C10orf105, CDH23
(V1369L)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely pathogenic