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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RTN4IP1
(P170S +1 more)
Single nucleotide variant
(missense variant)
Optic atrophy 10 with or without ataxia, intellectual disability, and seizures
GUncertain significance
RTN4IP1
(M1T)
Single nucleotide variant
(missense variant +2 more)
Optic atrophy 10 with or without ataxia, intellectual disability, and seizures
GPathogenic