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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBC1D24
(A289V)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 65
+3 more
GConflicting classifications of pathogenicity
TBC1D24
(W545* +1 more)
Single nucleotide variant
(nonsense)
Developmental and epileptic encephalopathy, 16
GLikely pathogenic