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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABBR2
(L736F)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 59
GUncertain significance
GABBR2
(S732I)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 59
GUncertain significance
GABBR2
(H355Q)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 59
GUncertain significance
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