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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNC
(G792C)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 56
+2 more
GConflicting classifications of pathogenicity
ASTN2, BRINP1
+19 more
Copy number loss
Intellectual disability, borderline
+5 more
GUncertain significance