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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LGI1
(S92L)
Single nucleotide variant
(missense variant +1 more)
Epilepsy, familial temporal lobe, 1
GUncertain significance
LGI1
(D157V +1 more)
Single nucleotide variant
(missense variant +1 more)
Seizure
+1 more
GUncertain significance