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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABBR2
(A567T)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
+5 more
GPathogenic
GABBR2
Single nucleotide variant
(intron variant)
Neurodevelopmental disorder with poor language and loss of hand skills
+2 more
GConflicting classifications of pathogenicity
GABBR2
Insertion
(nonsense)
Developmental and epileptic encephalopathy, 59
GLikely pathogenic
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