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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTOF
(E1062fs +2 more)
Duplication
(frameshift variant)
Autosomal recessive nonsyndromic hearing loss 9
GLikely pathogenic
OTOF
(R708*)
Single nucleotide variant
(nonsense)
Nonsyndromic genetic hearing loss
GPathogenic
OTOF
(R566W)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 9
+1 more
GUncertain significance
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