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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SZT2
Single nucleotide variant
(intron variant)
Developmental and epileptic encephalopathy, 18
GUncertain significance
SZT2
(A938T)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
+1 more
GUncertain significance
SZT2
(V1454I +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
+3 more
GBenign/Likely benign
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