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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GABRD
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
GABRD
(A331G)
Single nucleotide variant
(missense variant)
Epilepsy, idiopathic generalized, susceptibility to, 10
+1 more
GUncertain significance
GABRD
(G369S)
Single nucleotide variant
(missense variant)
Epilepsy, idiopathic generalized, susceptibility to, 10
+2 more
GUncertain significance
GABRD
(T401M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
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