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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DMXL2
(G1058R +1 more)
Single nucleotide variant
(missense variant +2 more)
Developmental and epileptic encephalopathy, 81
GUncertain significance
DMXL2
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance