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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDXR
(R257Q +6 more)
Single nucleotide variant
(missense variant +1 more)
Auditory neuropathy-optic atrophy syndrome
GUncertain significance
FDXR, LOC112533667
(M1V)
Single nucleotide variant
(missense variant +2 more)
Auditory neuropathy-optic atrophy syndrome
+1 more
GPathogenic/Likely pathogenic