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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC13A5
(G467fs +2 more)
Deletion
(frameshift variant +1 more)
Epileptic encephalopathy
GLikely pathogenic
SLC13A5
(L111R +1 more)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GLikely pathogenic