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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTOF
(Q833L +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
OTOF
(R82H)
Single nucleotide variant
(missense variant)
OTOF-related condition
+4 more
GConflicting classifications of pathogenicity
OTOF
(A21T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
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