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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDHAF1
(Y52*)
Single nucleotide variant
(nonsense)
Mitochondrial complex II deficiency, nuclear type 1
+2 more
GPathogenic/Likely pathogenic
LOC130064281, SDHAF1
Single nucleotide variant
(3 prime UTR variant)
Mitochondrial complex II deficiency, nuclear type 1
GUncertain significance
ALKBH6, APLP1
+79 more
Copy number loss
Generalized epilepsy with febrile seizures plus, type 1
GPathogenic
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