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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM1
(K315R)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 31
GUncertain significance
DNM1
Single nucleotide variant
(intron variant)
Developmental and epileptic encephalopathy, 31
+1 more
GPathogenic/Likely pathogenic