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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DEPDC5
(P470S +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial focal epilepsy with variable foci
+1 more
GUncertain significance
DEPDC5
(S1055del +6 more)
Microsatellite
(inframe_deletion +1 more)
Epilepsy, familial focal, with variable foci 1
GLikely pathogenic