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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTOGL
(M272fs +1 more)
Deletion
(frameshift variant)
Rare genetic deafness
+1 more
GPathogenic/Likely pathogenic
OTOGL
(G1639R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance