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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDXR
(T156M +6 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy
+1 more
GConflicting classifications of pathogenicity
FDXR
(Q115fs +4 more)
Deletion
(frameshift variant +2 more)
Auditory neuropathy-optic atrophy syndrome
GLikely pathogenic