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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDXR
(R399W +6 more)
Single nucleotide variant
(missense variant +1 more)
Optic atrophy
GUncertain significance
FDXR
(M296I +6 more)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
GUncertain significance
FDXR
(S246L +6 more)
Single nucleotide variant
(missense variant +1 more)
Retinal dystrophy
GUncertain significance
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