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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPA1
(K673del +9 more)
Microsatellite
(inframe_deletion)
Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)
GUncertain significance
OPA1
Deletion
(splice acceptor variant)
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
+8 more
GPathogenic/Likely pathogenic