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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABRG2
(T177N +8 more)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant nocturnal frontal lobe epilepsy
GLikely pathogenic
GABRG2
(Q217*)
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
GABRG2
(T90M +3 more)
Single nucleotide variant
(missense variant +1 more)
Febrile seizures, familial, 8
+2 more
GConflicting classifications of pathogenicity
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