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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNRNPU
(Q803* +1 more)
Single nucleotide variant
(nonsense)
Myoclonic absence seizure
+1 more
GBenign/Likely benign
HNRNPU
Single nucleotide variant
(splice acceptor variant)
Developmental and epileptic encephalopathy, 54
GLikely pathogenic
HNRNPU
(G422fs +1 more)
Deletion
(frameshift variant)
Developmental and epileptic encephalopathy, 54
GPathogenic
HNRNPU
Microsatellite
(nonsense)
Developmental and epileptic encephalopathy, 54
GPathogenic
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