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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COX6B1
(R20C)
Single nucleotide variant
(missense variant)
Mitochondrial complex IV deficiency, nuclear type 1
GLikely pathogenic
ARHGAP33, ATP4A
+44 more
Copy number loss
not provided
GPathogenic
ALKBH6, APLP1
+79 more
Copy number loss
Generalized epilepsy with febrile seizures plus, type 1
GPathogenic
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