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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABRB2
Single nucleotide variant
(synonymous variant)
Developmental and epileptic encephalopathy 92
+1 more
GUncertain significance
GABRB2
(R193H)
Single nucleotide variant
(missense variant)
Intellectual disability
+2 more
GConflicting classifications of pathogenicity
GABRB2
Deletion
(intron variant)
not provided
+1 more
GBenign
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