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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABRG2
(S114Y +5 more)
Single nucleotide variant
(missense variant)
Seizure
GUncertain significance
GABRG2
(A160D +8 more)
Single nucleotide variant
(missense variant)
Intellectual disability
GLikely pathogenic
GABRG2
(I169T +8 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability
GUncertain significance
GABRG2
(R323W +8 more)
Single nucleotide variant
(missense variant +1 more)
Epilepsy, childhood absence 2
+4 more
GConflicting classifications of pathogenicity
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