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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF3, LOC109115964
(G66C)
Single nucleotide variant
(missense variant)
Deafness with labyrinthine aplasia, microtia, and microdontia
GLikely pathogenic
FGF3, LOC109115964
(Y49C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC109115964, FGF3
(L6P)
Single nucleotide variant
(missense variant)
Deafness with labyrinthine aplasia, microtia, and microdontia
GPathogenic
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