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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABRD
(R416H)
Single nucleotide variant
(missense variant)
Epilepsy, idiopathic generalized, susceptibility to, 10
+1 more
GUncertain significance
GABRD
Single nucleotide variant
(3 prime UTR variant)
Epilepsy, idiopathic generalized, susceptibility to, 10
GUncertain significance