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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
JMJD1C, JMJD1C-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
Early myoclonic encephalopathy
+1 more
GLikely benign
JMJD1C, JMJD1C-AS1
(V19D)
Single nucleotide variant
(missense variant +2 more)
Early myoclonic encephalopathy
+1 more
GBenign/Likely benign