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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF13
(S17F +1 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 90
GUncertain significance
ABCD1, ADGRG4
+160 more
Copy number gain
not provided
GPathogenic